Überblick über die Statistik des Gehaltsniveaus für "Site Manager in Deutschland"

Location: Poland - Home based        Schedule: Freelance, Various FTEs                                    CROMSOURCE is a growing international CRO dedicated to a quality-focused approach with a collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Freelance Clinical Project Manager I, to join their clinical operations team in Poland. This is a full-time opportunity. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                      As a Project Manager, you will be responsible, for oversight of assigned clinical projects ensuring the quality of services in accordance with contractual obligations, applicable SOPs, ICH/GCP guidelines, and other, applicable regulations. You may also act as Project Director/Leader, depending on the complexity of the projects.   Join our team and help us deliver clinical trials that will improve patients' lives.                   Main Tasks and Responsibilities:Manages the development and planning of clinical projects, interacting with the Sponsor and the Investigators and coordinating the project team memberOversees the application process for clinical studies, in force in the country(ies) of work. Verifies the assigned project activities plan and timelines and the related critical stateManages the budget of the projectParticipates in Monitor's and Investigator's MeetingsProvides project updates to the Sponsor and to the Project Director/Leader and to the Clinical Department Director; participates in update meetings.Informs Project Director/Leader and the Clinical Department Director about any issues that can jeopardize the business relationship with the SponsorSupervises the team in relation to monitoring including submissions, site visits, ensuring compliance with ICH/GCP guidelines and applicable laws and regulationsUndertakes workload and performance assessments of the project team working with the Clinical Research Department Director to ensure adequate support levelsMay provide oversight and mentoring for junior staff assigned to the projects.Supervises the archiving activitiesSupervises, in the overall management of the project, the assigned Biometrics team and all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc…)Assists the Medical Monitor (MEM) in preparing protocols, Case Report Forms (CRFs), and final Clinical Study Reports (CSRs)Performs, if necessary, co-monitoring visits for the assigned clinical projectsMay act as Feasibility Associate (FEA) after appropriate and documented trainingMay prepare SOPs relating to clinical research activities in collaboration with the Quality System Unit (QSU)Arranges and collaborate with the assigned Clinical Research Department Director, in identifying the project-specific training of the project team and in delivering them Education and Experience:University Degree in scientific, medical, or paramedical disciplinesUp to three 3 years of project management experience in the CRO/Pharmaceutical industryStrong knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Application Process   Once you have submitted your CV, you will receive an acknowledgment email. If you have the requirements we need, you will be invited for a phone interview as the first step.        If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please contact [email protected] for more information.      Who will you be working for?      About CROMSOURCE      CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                      Our Company Ethos   Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates.      CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.      Keywords: Senior Project Manager, Clinical Project Manager, Senior Study Manager, Study Management Associate, Project Management Associate, Clinical, Drugs, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, CRO, Clinical Research Organisation, Contract Research Organisation  Skills: Clinical Project Manager, Clinical Study Manager, clinical trials, ICH-GCP, Project Management, EnglishLocation: PolandShare: LinkedIn Facebook Twitter Email

Site Manager*Position contingent upon award*Location: Germany – U.S. Government InstallationsContinuity Global Solutions (CGS) is pursuing a contract with a U.S. federal government agency to provide security at U.S. Army installations throughout Germany. Armed security personnel will provide static installation access control, roving security patrols, intrusion detection system monitoring, pass and badge control, static personal security and other security related functions as required. The armed security personnel will provide protection of U.S. Government installations, materials, property, and personnel.As part of this effort, CGS is looking for experienced Site Managers. The Site Managers will be responsible for the management and performance of the guard force at an assigned U.S. Army installation(s) and any satellite areas associated with the installation(s).Responsibilities:Responsible for effectively managing security operations and for Contractor (CGS) performance at assigned U.S. Army installationsPerforms direct line management of the armed guards assigned to the military installation(s)Responsible for quality control and for ensuring contract compliancePerforms accurate and detailed reporting Responsible for liaising with the client and with German authoritiesRequirementsSecurity or law enforcement administration experience in the armed forces, civilian police or commercial security agenciesThe above experience should demonstrate the capability to manage a program of comparable scope and magnitude (multiple guard teams operating simultaneously at different installations)Leadership experienceProject/program management experienceExperience managing armed security personnelExpertise in all areas of physical security and access controlComputer literacy, including the ability to use all common office management tools (e.g., Microsoft Office)Experience in basic communications and radio use/proceduresSecondary education or national diplomaMinimum five years of police, military and/or security management experience at the manager, supervisor or commander levelsMinimum two years of work experience in Germany)Intimate knowledge of overseas security environments and familiarity with specific threats in GermanyRisk management skills, including problem identification, risk management planning, qualitative risk analysis and problem solvingiability and good conduct on past assignmentsDesired Education & Experience:Secondary education or national diplomaMinimum five years of police, military and/or security management experience at the manager, supervisor or commander levelsMinimum two years of work experience in Germany)Intimate knowledge of overseas security environments and familiarity with specific threats in GermanyRisk management skills, including problem identification, risk management planning, qualitative risk analysis and problem solvingOther Required Qualifications:Professional fluency in both English & GermanMust be familiar with applicable U.S. military regulations and German lawsMust be a native-born citizen of a NATO-member country or a U.S. citizen (native-born or naturalized). Non-U.S. citizens are permitted only if they are ex-U.S. military or if they are a current U.S. military spouse/family member. Active-duty service members are not eligible.Must meet, or be eligible to meet, security criteria in accordance with AER 190-16 requirements, AE Form 604-1A and 604-1B, IAW AE Regulation 604-1, Local National Screening Program in Germany (LNSP)Must be able to pass a background check (e.g., European Police Good Conduct Certificates (EPGCC) for EU citizens or a German PGCC; a National Crime Information Center (NCIC) Check – Interstate Identification Index (NCIC-III) for U.S. citizens; or AE Form 190-45D for U.S. military family members/DoD civiliansMust be a resident of Germany for 12 consecutive months at the time of contract awardMust be willing to sign a Letter of Commitment with CGSMust be capable of maintaining a professional demeanor under highly stressful circumstancesMust have a verifiable record of proven reliability and good conduct on past assignmentsRequirementsSecondary education or national diplomaMinimum five years of police, military and/or security management experience at the manager, supervisor or commander levelsMinimum two years of work experience in Germany)Professional fluency in both English & GermanMust be familiar with applicable U.S. military regulations and German lawsMust be a native-born citizen of a NATO-member country or a U.S. citizen (native-born or naturalized). Non-U.S. citizens are permitted only if they are ex-U.S. military or if they are a current U.S. military spouse/family member. Active-duty service members are not eligible.Must meet, or be eligible to meet, security criteria in accordance with AER 190-16 requirements, AE Form 604-1A and 604-1B, IAW AE Regulation 604-1, Local National Screening Program in Germany (LNSP)Must be able to pass a background check (e.g., European Police Good Conduct Certificates (EPGCC) for EU citizens or a German PGCC; a National Crime Information Center (NCIC) Check – Interstate Identification Index (NCIC-III) for U.S. citizens; or AE Form 190-45D for U.S. military family members/DoD civiliansMust be a resident of Germany for 12 consecutive months at the time of contract awardMust be willing to sign a Letter of Commitment with CGSMust be capable of maintaining a professional demeanor under highly stressful circumstancesMust have a verifiable record of proven reliability and good conduct on past assignmentsÜber das Unternehmen:Continuity Global Solutions

Site Manager*Position contingent upon award*Location: Germany – U.S. Government InstallationsContinuity Global Solutions (CGS) is pursuing a contract with a U.S. federal government agency to provide security at U.S. Army installations throughout Germany. Armed security personnel will provide static installation access control, roving security patrols, intrusion detection system monitoring, pass and badge control, static personal security and other security related functions as required. The armed security personnel will provide protection of U.S. Government installations, materials, property, and personnel.As part of this effort, CGS is looking for experienced Site Managers. The Site Managers will be responsible for the management and performance of the guard force at an assigned U.S. Army installation(s) and any satellite areas associated with the installation(s).Responsibilities:Responsible for effectively managing security operations and for Contractor (CGS) performance at assigned U.S. Army installationsPerforms direct line management of the armed guards assigned to the military installation(s)Responsible for quality control and for ensuring contract compliancePerforms accurate and detailed reporting Responsible for liaising with the client and with German authoritiesRequirementsSecurity or law enforcement administration experience in the armed forces, civilian police or commercial security agenciesThe above experience should demonstrate the capability to manage a program of comparable scope and magnitude (multiple guard teams operating simultaneously at different installations)Leadership experienceProject/program management experienceExperience managing armed security personnelExpertise in all areas of physical security and access controlComputer literacy, including the ability to use all common office management tools (e.g., Microsoft Office)Experience in basic communications and radio use/proceduresSecondary education or national diplomaMinimum five years of police, military and/or security management experience at the manager, supervisor or commander levelsMinimum two years of work experience in Germany)Intimate knowledge of overseas security environments and familiarity with specific threats in GermanyRisk management skills, including problem identification, risk management planning, qualitative risk analysis and problem solvingiability and good conduct on past assignmentsDesired Education & Experience:Secondary education or national diplomaMinimum five years of police, military and/or security management experience at the manager, supervisor or commander levelsMinimum two years of work experience in Germany)Intimate knowledge of overseas security environments and familiarity with specific threats in GermanyRisk management skills, including problem identification, risk management planning, qualitative risk analysis and problem solvingOther Required Qualifications:Professional fluency in both English & GermanMust be familiar with applicable U.S. military regulations and German lawsMust be a native-born citizen of a NATO-member country or a U.S. citizen (native-born or naturalized). Non-U.S. citizens are permitted only if they are ex-U.S. military or if they are a current U.S. military spouse/family member. Active-duty service members are not eligible.Must meet, or be eligible to meet, security criteria in accordance with AER 190-16 requirements, AE Form 604-1A and 604-1B, IAW AE Regulation 604-1, Local National Screening Program in Germany (LNSP)Must be able to pass a background check (e.g., European Police Good Conduct Certificates (EPGCC) for EU citizens or a German PGCC; a National Crime Information Center (NCIC) Check – Interstate Identification Index (NCIC-III) for U.S. citizens; or AE Form 190-45D for U.S. military family members/DoD civiliansMust be a resident of Germany for 12 consecutive months at the time of contract awardMust be willing to sign a Letter of Commitment with CGSMust be capable of maintaining a professional demeanor under highly stressful circumstancesMust have a verifiable record of proven reliability and good conduct on past assignmentsRequirementsSecondary education or national diplomaMinimum five years of police, military and/or security management experience at the manager, supervisor or commander levelsMinimum two years of work experience in Germany)Professional fluency in both English & GermanMust be familiar with applicable U.S. military regulations and German lawsMust be a native-born citizen of a NATO-member country or a U.S. citizen (native-born or naturalized). Non-U.S. citizens are permitted only if they are ex-U.S. military or if they are a current U.S. military spouse/family member. Active-duty service members are not eligible.Must meet, or be eligible to meet, security criteria in accordance with AER 190-16 requirements, AE Form 604-1A and 604-1B, IAW AE Regulation 604-1, Local National Screening Program in Germany (LNSP)Must be able to pass a background check (e.g., European Police Good Conduct Certificates (EPGCC) for EU citizens or a German PGCC; a National Crime Information Center (NCIC) Check – Interstate Identification Index (NCIC-III) for U.S. citizens; or AE Form 190-45D for U.S. military family members/DoD civiliansMust be a resident of Germany for 12 consecutive months at the time of contract awardMust be willing to sign a Letter of Commitment with CGSMust be capable of maintaining a professional demeanor under highly stressful circumstancesMust have a verifiable record of proven reliability and good conduct on past assignmentsÜber das Unternehmen:Continuity Global Solutions

Location: Italy - Home or office based      Schedule: Permanent, Full-time                 Do you want to join a team that is passionate about making a difference in drug and medical device development?  CROMSOURCE, a growing CRO, is recruiting for a Senior Clinical Project Manager to join their clinical operations team. This is a permanent opportunity in Italy. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                          As a Senior Clinical Project Manager, you will be responsible, for oversight of assigned clinical projects ensuring the quality of services in accordance with contractual obligations, applicable SOPs, ICH/GCP guidelines, and other, applicable regulations. You may also act as Project Director/Leader, depending on the complexity of the projects. Previous experience with respiratory and oncology trials is preferred. A minimum of 3 years of experience with a CRO is needed.           Join our team and help us deliver clinical trials that will improve patients' lives.                               Main Tasks and Responsibilities:Manages the development and planning of clinical projects, interacting with the Sponsor and the Investigators, and coordinating the project team members.Oversees the application process for clinical studies, in force in the country(ies) of work. Verifies the assigned project activities plan and timelines and the related critical state.Manages the budget of the project.Participates in Monitor's and Investigator's MeetingsProvides project updates to the Sponsor and to the Project Director/Leader and to the Clinical Department Director; participates in update meetings.Informs Project Director/Leader and the Clinical Department Director about any issues that can jeopardize the business relationship with the Sponsor.Supervises the team in relation to monitoring including submissions, site visits, ensuring compliance with ICH/GCP guidelines and applicable laws and regulations.Undertakes workload and performance assessments of the project team working with the Clinical Research Department Director to ensure adequate support levels.May provide oversight and mentoring for junior staff assigned to the projects.Supervises the archiving activities.Supervises, in the overall management of the project, the assigned Biometrics team and all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc…)Assists the Medical Monitor (MEM) in preparing protocols, Case Report Forms (CRFs), and final Clinical Study Reports (CSRs)Performs, if necessary, co-monitoring visits for the assigned clinical projects.May act as Feasibility Associate (FEA) after appropriate and documented training.May prepare SOPs relating to clinical research activities in collaboration with the Quality System Unit (QSU)Arranges and collaborate with the assigned Clinical Research Department Director, in identifying the project-specific training of the project team and in delivering them. Education and Experience Required:University Degree in scientific, medical, or paramedical disciplines with 3 years of experienceSignificant 3 years of experience in clinical project management in the CRO/pharmaceutical industryExcellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel. The Benefits of Working in Italy:· Meal vouchers· Mobile phone if requested by the Line Manager· Dedicated Line Manager Who will you be working for?                                    About CROMSOURCE                       CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                                                    Our Company Ethos                  Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they can develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below-industry average turnover rates.                                     The Application Process                  Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements we need, you will be invited for a phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.               If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please contact [email protected] for more information.                                        CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.                                     Keywords: Project Manager, Clinical Project Manager, CRO, Clinical Research Organisation, Contract Research Organisation, Clinical, Drugs, Medical Devices, Medical Device, Project Management, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, Respiratory, Oncology, OphthalmologySkills: Clinical Project Manager, Clinical Study Manager, Clinical Trial Manager, Senior Clinical Project Manager, clinical trials, CRO, Medical Devices, Study ManagementLocation: ItalyShare: LinkedIn Facebook Twitter Email

Location: Spain - Home-based          Schedule: Permanent, Full-time                         Do you want to join a team that is passionate about making a difference in drug and medical device development?  CROMSOURCE, a growing CRO, is recruiting for a Senior Clinical Project Manager to join their clinical operations team. This is a permanent opportunity in Spain. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                                  As a Senior Clinical Project Manager, you will be responsible, for oversight of assigned clinical projects ensuring the quality of services in accordance with contractual obligations, applicable SOPs, ICH/GCP guidelines, and other, applicable regulations. You may also act as Project Director/Leader, depending on the complexity of the projects. Previous experience with respiratory and oncology trials is preferred. A minimum of 3 years of experience with a CRO is needed.                   Join our team and help us deliver clinical trials that will improve patients' lives.                                         Main Tasks and Responsibilities:Manages the development and planning of clinical projects, interacting with the Sponsor and the Investigators, and coordinating the project team members.Oversees the application process for clinical studies, in force in the country(ies) of work. Verifies the assigned project activities plan and timelines and the related critical state.Manages the budget of the project.Participates in Monitor's and Investigator's MeetingsProvides project updates to the Sponsor and to the Project Director/Leader and to the Clinical Department Director; participates in update meetings.Informs Project Director/Leader and the Clinical Department Director about any issues that can jeopardize the business relationship with the Sponsor.Supervises the team in relation to monitoring including submissions, site visits, ensuring compliance with ICH/GCP guidelines and applicable laws and regulations.Undertakes workload and performance assessments of the project team working with the Clinical Research Department Director to ensure adequate support levels.May provide oversight and mentoring for junior staff assigned to the projects.Supervises the archiving activities.Supervises, in the overall management of the project, the assigned Biometrics team and all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Assists the Medical Monitor (MEM) in preparing protocols, Case Report Forms (CRFs), and final Clinical Study Reports (CSRs)Performs, if necessary, co-monitoring visits for the assigned clinical projects.May act as Feasibility Associate (FEA) after appropriate and documented training.May prepare SOPs relating to clinical research activities in collaboration with the Quality System Unit (QSU)Arranges and collaborate with the assigned Clinical Research Department Director, in identifying the project-specific training of the project team and in delivering them. Education and Experience Required:University Degree in scientific, medical, or paramedical disciplines with 3 years of experienceSignificant 3 years of experience in clinical project management in the CRO/pharmaceutical industryExcellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel  The Benefits of Working in Spain:Competitive SalaryHealth insuranceHome office allowanceMeal vouchers23 days of holiday per yearDedicated Line Manager Who will you be working for?                                             About CROMSOURCE                            CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                                                              Our Company Ethos                       Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they can develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below-industry average turnover rates.                                             The Application Process                       Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements we need, you will be invited for a phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.                       If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please contact [email protected] for more information.                                                  CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.                                             Keywords: Project Manager, Clinical Project Manager, CRO, Clinical Research Organisation, Clinical, Drugs, Medical Devices, Medical Device, Project Management, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, Respiratory, Oncology, OphthalmologySkills: Clinical Project Manager, Clinical Study Manager, Clinical Trial Manager, Senior Clinical Project Manager, Senior Clinical Trial Manager, clinical trials, CRO, Medical Devices, Study ManagementLocation: SpainShare: LinkedIn Facebook Twitter Email

Location: Germany- Home or office based      Schedule: Permanent, Full-time                 Do you want to join a team that is passionate about making a difference in drug and medical device development? CROMSOURCE, a growing CRO, is recruiting for a Senior Clinical Project Manager to join their clinical operations team. This is a permanent opportunity in Germany. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                          As a Senior Clinical Project Manager, you will be responsible, for oversight of assigned clinical projects ensuring the quality of services in accordance with contractual obligations, applicable SOPs, ICH/GCP guidelines, and other, applicable regulations. You may also act as Project Director/Leader, depending on the complexity of the projects. Previous experience with respiratory and oncology trials is preferred. A minimum of 3 years of experience with a CRO is needed.           Join our team and help us deliver clinical trials that will improve patients' lives.                                 Main Tasks and Responsibilities:Manages the development and planning of clinical projects, interacting with the Sponsor and the Investigators, and coordinating the project team members.Oversees the application process for clinical studies, in force in the country(ies) of work. Verifies the assigned project activities plan and timelines and the related critical state.Manages the budget of the project.Participates in Monitor's and Investigator's MeetingsProvides project updates to the Sponsor and to the Project Director/Leader and to the Clinical Department Director; participates in update meetings.Informs Project Director/Leader and the Clinical Department Director about any issues that can jeopardize the business relationship with the Sponsor.Supervises the team in relation to monitoring including submissions, site visits, ensuring compliance with ICH/GCP guidelines and applicable laws and regulations.Undertakes workload and performance assessments of the project team working with the Clinical Research Department Director to ensure adequate support levels.May provide oversight and mentoring for junior staff assigned to the projects.Supervises the archiving activities.Supervises, in the overall management of the project, the assigned Biometrics team and all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc…)Assists the Medical Monitor (MEM) in preparing protocols, Case Report Forms (CRFs), and final Clinical Study Reports (CSRs)Performs, if necessary, co-monitoring visits for the assigned clinical projects.May act as Feasibility Associate (FEA) after appropriate and documented training.May prepare SOPs relating to clinical research activities in collaboration with the Quality System Unit (QSU)Arranges and collaborate with the assigned Clinical Research Department Director, in identifying the project-specific training of the project team and in delivering them. Education and Experience Required:University Degree in scientific, medical, or paramedical disciplines with 3 years of experienceSignificant 3 years of experience in clinical project management in the CRO/pharmaceutical industryExcellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel. The Benefits of Working in Germany:30 Euro net Internet cost reimbursement per monthAdditional Accident Insurance, fully covered by the company.25 vacation daysPossibility of salary conversion for additional pension insuranceDedicated Line ManagerMonthly meetings with the line managerFull performance and development process with end-of-year reviewsTeam events and end-of-year partyCareer opportunities within both our CRO departments and our TalentSource Life Sciences Unit, locally and internationallyEmployee satisfaction survey - your feedback is important for continuous improvement. Who will you be working for?                                    About CROMSOURCE                        CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                                                      Our Company Ethos                  Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they can develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below-industry average turnover rates.                                     The Application Process                  Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements we need, you will be invited for a phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.               If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please contact [email protected] for more information.                                          CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.                                     Keywords: Project Manager, Clinical Project Manager, CRO, Clinical Research Organisation, Contract Research Organisation, Clinical, Drugs, Medical Devices, Medical Device, Project Management, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, Respiratory, Oncology, OphthalmologySkills: Clinical Project Manager, Clinical Trial Manager, clinical trials, CRO, Medical Devices, Project Leadership, Project ManagementLocation: GermanyShare: LinkedIn Facebook Twitter Email

GEBHARDT Intralogistics GroupDie GEBHARDT Intralogistics Group ist einer der führenden Anbieter von Materialfluss- und innerbetrieblichen Logistiksystemen. Seit 70 Jahren entwickelt GEBHARDT maßgeschneiderte Komplettlösungen – von der Idee bis zur vollständigen Realisierung – im Bereich Transport, Materialfluss, Sortiertechnik, Montage- und Lagertechnik, einschließlich Steuerung & Automatisierung, Lagerverwaltungssysteme und IT-Integration.GEBHARDT Intralogistics GroupDie GEBHARDT Intralogistics Group ist einer der führenden Anbieter von Materialfluss- und innerbetrieblichen Logistiksystemen. Seit 70 Jahren entwickelt GEBHARDT maßgeschneiderte Komplettlösungen – von der Idee bis zur vollständigen Realisierung – im Bereich Transport, Materialfluss, Sortiertechnik, Montage- und Lagertechnik, einschließlich Steuerung & Automatisierung, Lagerverwaltungssysteme und IT-Integration.FÄHIGKEITEN, DIE BENÖTIGT WERDEN/YOUR CAPABILITIES:English version below:Abgeschlossene Ausbildung im technischen und industriellen Bereich sowie entsprechende Weiterbildung zum Techniker/Meister oder vergleichbare QualifikationenMehrjährige Erfahrung in Installation und Inbetriebnahme im Automationssektor (bevorzugt Förder- und Lagersysteme)Erfahrung im Umgang mit Kunden und der Pflege von KundenbeziehungenInitiative, Flexibilität, eigenständiges und lösungsorientiertes Arbeiten sowie ausgeprägte, nachgewiesene organisatorische und FührungsfähigkeitenGute Beherrschung von Englisch und Französisch in Wort und Schrift, weitere Sprachkenntnisse, wie Deutsch, sind von Vorteil__________________________________________________________________________Completed technical and industrial apprenticeship and further training as a technician/master craftsman or comparable qualificationsMany years of experience in installation and commissioning in the automation sector (preferably conveyor and warehouse systems)Initiative, flexible, independent, and solution-orientedProven organizational and leadership skillsGood command of written and spoken English and Frensh, further language skills are an advantage. German language skills are advantageousAUFGABEN, DIE AUF SIE WARTEN/YOUR TASKS:English version below:Verantwortlich für die Ausführung und Überwachung der Baustelle eines Automatisierungsprojekts in Frankreich (Region Lille)Eröffnung der Baustelle (Büro, IT-Ausstattung, Arbeitsgenehmigungen, Eintrittsgenehmigungen usw.) unter Berücksichtigung des Vertrags, der Spezifikationen und der Kunden-/ProjektstandardsVerantwortlich für die Leitung eines Abschnitts der Baustelle und Anweisung und Anleitung der Mitarbeiter (intern und extern) hinsichtlich Arbeitssicherheitsbestimmungen, Kontrolle der Arbeitsergebnisse usw.Zusammen mit dem Sicherheitsspezialisten verantwortlich für die Arbeitssicherheit auf der Baustelle und Erstellung und Pflege aktueller RisikobewertungenVerantwortlich für die Durchführung und Überwachung der Implementierungsarbeiten: Dies umfasst die Ausführung der mechanischen und elektrischen Installation sowie die Inbetriebnahme in Bezug auf Inhalt und PersonalDefinition und Überwachung der Implementierungssequenz und -zeitplanung vor Ort unter Berücksichtigung des Einführungszeitplans des KundenZentraler Ansprechpartner für den Kunden und Projektleiter für den BaustellenabschnittErfassung und Bewertung von Über- und Untererfüllungen und Kommunikation dieser an das ProjektmanagementVerantwortlich für alle logistischen Belange auf der Baustelle__________________________________________________________________________Responsible for the execution and supervision of the installation of an Automation project in France (Lille area)Planning and preparing the construction site (office, IT supplies, work passes, entry permits, etc.) considering the contract, specifications and the customer/project standardsResponsible for the management of the installation on site. Monitoring the onsite installation sequence and schedule, taking into account the customer’s launch dateInstructing and guiding employees (internal & external) with regards to safety regulations. Together with the safety specialist, responsible for occupational safety on the construction site and create and maintain current risk assessmentsMonitoring the installation: This includes the execution of the mechanical & electrical installation and commissioning, in terms of content and personnelMain contact person to the customer and project manager on the construction siteRegularly report to the Turnkey project managementResponsible for all logistics related to the siteLEISTUNGEN, DIE WIR BIETEN:Wir bieten Ihnen einen modernen Arbeitsplatz in einem stark expandierenden Unternehmen mit einer abwechslungsreichen interessanten Aufgabenstellung. Wir suchen eine selbstständige, verantwortungsbewusste Verstärkung, die sich gut in unser Team einfügt und den weiteren Ausbau unseres Unternehmens kreativ mitgestaltet.Verantwortlichkeiten:English version below:Verantwortlich für die Ausführung und Überwachung der Baustelle eines Automatisierungsprojekts in Frankreich (Region Lille)Eröffnung der Baustelle (Büro, IT-Ausstattung, Arbeitsgenehmigungen, Eintrittsgenehmigungen usw.) unter Berücksichtigung des Vertrags, der Spezifikationen und der Kunden-/ProjektstandardsVerantwortlich für die Leitung eines Abschnitts der Baustelle und Anweisung und Anleitung der Mitarbeiter (intern und extern) hinsichtlich Arbeitssicherheitsbestimmungen, Kontrolle der Arbeitsergebnisse usw.Zusammen mit dem Sicherheitsspezialisten verantwortlich für die Arbeitssicherheit auf der Baustelle und Erstellung und Pflege aktueller RisikobewertungenVerantwortlich für die Durchführung und Überwachung der Implementierungsarbeiten: Dies umfasst die Ausführung der mechanischen und elektrischen Installation sowie die Inbetriebnahme in Bezug auf Inhalt und PersonalDefinition und Überwachung der Implementierungssequenz und -zeitplanung vor Ort unter Berücksichtigung des Einführungszeitplans des KundenZentraler Ansprechpartner für den Kunden und Projektleiter für den BaustellenabschnittErfassung und Bewertung von Über- und Untererfüllungen und Kommunikation dieser an das ProjektmanagementVerantwortlich für alle logistischen Belange auf der Baustelle__________________________________________________________________________Responsible for the execution and supervision of the installation of an Automation project in France (Lille area)Planning and preparing the construction site (office, IT supplies, work passes, entry permits, etc.) considering the contract, specifications and the customer/project standardsResponsible for the management of the installation on site. Monitoring the onsite installation sequence and schedule, taking into account the customer’s launch dateInstructing and guiding employees (internal & external) with regards to safety regulations. Together with the safety specialist, responsible for occupational safety on the construction site and create and maintain current risk assessmentsMonitoring the installation: This includes the execution of the mechanical & electrical installation and commissioning, in terms of content and personnelMain contact person to the customer and project manager on the construction siteRegularly report to the Turnkey project managementResponsible for all logistics related to the siteQualifikationen:English version below:Abgeschlossene Ausbildung im technischen und industriellen Bereich sowie entsprechende Weiterbildung zum Techniker/Meister oder vergleichbare QualifikationenMehrjährige Erfahrung in Installation und Inbetriebnahme im Automationssektor (bevorzugt Förder- und Lagersysteme)Erfahrung im Umgang mit Kunden und der Pflege von KundenbeziehungenInitiative, Flexibilität, eigenständiges und lösungsorientiertes Arbeiten sowie ausgeprägte, nachgewiesene organisatorische und FührungsfähigkeitenGute Beherrschung von Englisch und Französisch in Wort und Schrift, weitere Sprachkenntnisse, wie Deutsch, sind von Vorteil__________________________________________________________________________Completed technical and industrial apprenticeship and further training as a technician/master craftsman or comparable qualificationsMany years of experience in installation and commissioning in the automation sector (preferably conveyor and warehouse systems)Initiative, flexible, independent, and solution-orientedProven organizational and leadership skillsGood command of written and spoken English and Frensh, further language skills are an advantage. German language skills are advantageousÜber das Unternehmen:GEBHARDT FördertechnikBranche:Project managementWebsite:https://www.linkedin.com/company/gebhardt-f-rdertechnik-gmbh/>>>>>https://www.facebook.com/GEBHARDT.intralogistics.group/>>>>>https://twitter.com/GebhardtGroup

Wer wir sindDie HGK Shipping ist das führende Binnenschifffahrtsunternehmen in Europa. Wir sind wegweisender Partner in der Trocken-, Gas- und Chemieschifffahrt. Mit einem Flottenbestand von über 350 eigenen und gecharterten Binnenschiffen befördern wir pro Jahr etwa 43 Mio. Tonnen Fracht. Im Verbund der HGK Gruppe kombinieren wir durch moderne Konzepte die Verkehrsträger Schiene, Wasserwege und Straße zu nachhaltigen Transportketten und sind Teil einer der führenden Akteure im intermodalen Güterverkehr. Mehr als 2500 Menschen arbeiten heute von Rotterdam bis Basel unter dem Dach der HGK-Gruppe. Für unsere Business Unit Ship Management am Standort Duisburgsuchen wir Sie zum frühestmöglichen Zeitpunkt unbefristet in Vollzeit (40 Std.) als Technical Superintendent Dry Ihre AufgabenTechnische Betreuung von definierten Fahrzeugeinheiten (motorisiert & nicht motorisiert) der Trockengüterschifffahrts-FlotteTechnische Betreuung unserer Umschlag- und Lageranlagen in Kooperation mit Kollegen on- und off-siteBeurteilen des technischen Zustands der Flotte und weiterer Anlagen durch regelmäßige Bord-/VorortbesuchePlanen, Budgetieren, Durchführen und Überwachen von Wartungs-, Instandhaltungs-, Attest- und Investitionsmaßnahmen Unterstützung des Manager Fleet bei der Erarbeitung von Ausschreibungsunterlagen sowie der Nachkalkulation von Projekten Beauftragen, begleiten und überwachen von Dienstleistern und Lieferanten Unterstützung der kommerziellen und operativen Bereiche bei technischen FragestellungenUnterstützung und Zusammenarbeit mit der Abteilung QEHS und ArbeitssicherheitIhr ProfilSie haben ein abgeschlossenes Studium (B.Sc./Dipl.-Ing.) in der Fachrichtung Schiffbau, Schiffsmaschinenbau oder Schiffstechnik und Sie können erste praktische Erfahrungen vorweisen alternativ haben Sie langjährige Erfahrung als Schiffsführer und nachweislich Kenntnisse im Bereich der Wartung- und Instandhaltung von schiffstechnischen Anlagen und Maschinen alternativ haben Sie Erfahrung als Projektmanager an einer Schiffswerft oder einem der Schifffahrt nahen GewerbezweigSie besitzen eine Hands-on-Mentalität und sind flexibelSie verfügen über einen sicheren Umgang mit gängigen MS-Office-Anwendungen Sie haben ein Faible für technische Innovationen und sind aufgeschlossen für Neuerungen Sie sind teamfähig, überzeugen durch Kommunikationsgeschick auf unterschiedlichen Verantwortungsebenen, sicheres Auftreten und OrganisationstalentSie sind engagiert, zuverlässig, sorgfältig und schätzen eine selbstständige ArbeitsweiseDeutsch und Englisch beherrschen Sie in Wort und SchriftUnser AngebotWir bieten Ihnen interessante sowie anspruchsvolle Tätigkeiten in einem international wachsenden Unternehmen. Es erwarten Sie ein angenehmes Arbeitsklima in einem sympathischen Team, individuelle Entwicklungs- und Weiterbildungsmöglichkeiten sowie langfristige Perspektiven. Neben einer attraktiven Vergütung bieten wir Ihnen umfangreiche Sozialleistungen.Interesse?Dann freuen wir uns auf Ihre vollständige Bewerbung. Bitte bewerben Sie sich ausschließlich über unser Jobportal unter Angabe Ihrer Gehaltsvorstellung und Verfügbarkeit.Ihre Daten werden für den Bewerbungsprozess elektronisch gespeichert, verarbeitet und genutzt. Nach Abschluss des Bewerbungsprozesses löschen wir Ihre Daten spätestens nach 6 Monaten, sofern Sie keiner weiteren Speicherung zustimmen.HGK Shipping GmbHSarah Mantler / HR Business PartnerTelefon +49 203 3958 7112 Standort HGK Shipping - Karriere, Düsseldorf

Job Posting Title: Outfitting Manager (Cruise Ship) Req ID: 10050613 Job Description: Walt Disney Imagineering makes the impossible possible, by combining innovation and storytelling to bring Disney stories, characters and worlds to life. Imagineering is the master planning, creative development, design, engineering, production, project management, and research and development arm of Disney’s Parks and Resorts business segment. Representing more than 150 subject areas, its dedicated teams of Imagineers are responsible for the creation - from concept initiation through installation and commissioning - of all Disney Resorts, theme parks and attractions, cruise ships, real estate developments, regional entertainment venues, and new media projects. Disney Imagineers are passionate individuals that bring together the best aspects of creativity, innovation, and passion. The Outfitting Manager collaborates closely with various stakeholders to ensure smooth project execution. With keen attention to detail and strong organizational skills, you will ensure that all outfitting activities align with the established timeline and budget. What You Will Do Evaluates risk early in project and provides strategic thinking expertise during pre-construction Identifies and monitors applicable points of coordination at multiple levels Arbitrates on-site conflicts between vendors Takes the lead on ensuring work in the field meets quality requirements of contract documents, applicable codes, and to WDI / DPEP / DCL / Worldwide Safety Standards / SOLAS / ADA / USPH Attending inspections with MTO onboard to ensure design compliance with cabling, AC, wall and ceiling closures, deck penetrations, etc.... Alert PM of any conflicts/site issues and collaborate on solutions to keep spirit of design intact Critically review outfitter procurement log and compare it with outfitter and shipyard schedules Coordinate outfitter construction between adjacent spaces to ensure scope is understood. Attend daily meetings with shipyard to answer questions from builder, inform shipyard of issues from the PM, communicate to builder upcoming owner activities, and coordinate schedules accordingly Attend weekly outfitter, PM, and yard meetings to be aware of owner issues Enforces the safety program in close coordination with WDI / DPEP / Worldwide Safety / Shipyard, including maintaining a clean and organized job site Provides constructability analysis and value engineering recommendations Prepares weekly log of contractor work activities and reports to project planner Assures shipyard compliance with contract drawings and specifications Lead site logistics planning and setting up staging locations onboard in coordination with internal logistics team, other CMs, DCL, and shipyard Establishes and maintains project photo documentation including updating StructionSite at a regular cadence Manages commissioning through turnover acceptance Participates in FATs at contractor/vendor sites Drives critical path, schedule, KSMs, and Milestone compliance —elevates to leaders as needed Communication / Influence: Strong influence on project/site decisions Arbitrates on-site conflicts between contractors Communicates / collaborates with the design team on a daily basis to review submittals and site delivered material for compliance to contract documents Leads communication, coordinates, and collaborates project specific priorities with shipyard, outfitters, vendors, consultants, project planner, and project team members Qualifications: 3+ years field experience in applicable cruise ship development Strong organization and tracking skills Collaboration and relationship building Conflict Management Ability to lead Pull Planning & collaborate with Planner / Scheduler Manage multiple priorities Justification For Change/Directive writing Technical experience and expertise in all areas of construction field activities Ability to read and interpret construction drawings and specifications Competent in Office and project related software for given intended project: BIM 360 Field/Glue/Documents, Bluebeam, BOX, etc. Project management (document control) platforms for CRI/Submittal management, Enovia, SAP, Smartsheet, etc. #LI-JB4 Job Posting Segment: WDI Delivery Job Posting Primary Business: Project Design & Delivery (WDI) Primary Job Posting Category: Project/Program Management Generalist Employment Type: Full time Primary City, State, Region, Postal Code: Papenburg, Germany Alternate City, State, Region, Postal Code: Date Posted: 2023-07-11 Learn more about us.Über das Unternehmen:2214 Walt Disney Imagineering (Germany) GmbH

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. Position Summary: Responsible for study oversight and delivery management (time, budget, quality) at country level from start-up to closure. Serves as the main point of contact at a country level for internal and external stakeholders. Position Responsibilities: Coordinates country cross functional teams and acts as the main point of contact for a Country with the protocol manager and other global study team members Coordinates with other internal roles in country and site feasibility process, including proposal and validation of country study targets Develops country level patient recruitment strategy & risk mitigation. Coordinates and ensures country level study enrolment targets and timelines are met Leads problem solving and resolution efforts including management of risk, contingencies, issue resolution and escalation to the appropriate stakeholder/s Assessment and set up the of vendors during study start up period (locally) Investigator Meeting participation and preparation Ensures data entered in Clinical Trial Managements Systems is current and complete and access to eDC and vendor systems is available for the Country and clinical trial site personnel Validation of study related materials (i.e. protocol, ICF, patient material) Responsible for preparing country specific documents (e.g. global country specific amendment) Prepares materials for Site Initiation Visits Responsible for verifying and confirming with local team eTMF completeness (Country and Site level) Reviews Site Monitoring visit reports, takes action within the timelines specified and escalates issues and ensures appropriate documentation of issues. Coordination of database locks and query follow up. Ensures timelines are met. Ensure inspection readiness of assigned trials within country. Provide support to Health Authority inspection and pre-inspection activities Coordinates, develops and writes the Corrective Actions / Preventive Actions (CAPA) and ensures implementation for Country audit level findings. Drives CAPA review, implementation and completion. Lead study team meetings locally Reviewing and approving payments (based on GOA) and manage patient compensation claims (if applicable) Management of Site relationships (includes CRO related issues) May conduct Pre-Study Evaluation Visits (PSEVs) and Site Initiation Visits (SIVs) May perform site closure activities, including post-close out May act as point of contact for Sites May support preparing submissions to and obtaining approval from local Health Authorities, Ethics Committees and other relevant instances. Depending on the experience and previous knowledge of the specific candidate, the position may be adjusted to the Senior Level. Senior Level Expectations: Engage with Protocol Manager, line management and/or Head of Clinical Operations to assist in the resolution of complex issues both locally and/or globally Serve as a key resource for colleagues, by providing guidance, leading training and mentoring to other team members through a mentoring process using informal and/or formal presentations (Disclaimer: The responsibilities listed above are only a summary and other responsibilities will be requirements as assigned) Position Requirements: Degree Requirements: Bachelors or Masters degree required. Field of study within life sciences or equivalent Experience Requirements: Clinical Trial Manager: Minimum of 4 years' industry related experience Senior Clinical Trial Manager: At least 6 years of industry related experience Experience in leading or participating as an active member of cross functional teams, task forces, or local and global initiatives Key Competency Requirements: Thorough understanding of GCP, ICH Guidelines and Country regulatory environment In depth knowledge and understanding of clinical research processes, regulations and methodology Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management Demonstrated organizational and planning skills and independent decision-making ability Strong organization and time management skills and ability to effectively manage multiple competing priorities Ability of critical thinking and risk analysis. Strong communication skills with a strong customer focus, able to manage both internal and external clients at all organizational levels Skilled in the use of technology Good verbal and written communication skills (both in English and local language). Software that must be used independently and without assistance (e.g., Microsoft Suite): Microsoft Suite Clinical Trial Management Systems (CTMS) Electronic Data Capture Systems (eDC) Electronic Trial Master File (eTMF) Based on your function, department or individual position, you will have the opportunity to discuss with your Manager the option to work remotely up to 50% of the time, over a two-week period, with the flexibility to choose the days that align with your collaboration needs. This fixed-term role is meant as maternity cover until 30.06.2025. #LI-Hybrid If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to **********. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.Über das Unternehmen:0044 BMS GmbH&Co.KGaA Germany

Wir suchen einen Medical Science Liaison Manager (m/w/d) in der Nephrologie für das Gebiet Würzburg-Stuttgart-Freiburg-Ulm zur Verstärkung unserer Abteilung Medizin zum nächstmöglichen Zeitpunkt. Als Medical Science Liaison Manager (m/w/d) betreuen Sie Ihr eigenes Gebiet und sind erster Ansprechpartner für Entscheidungsträger in Kliniken und Niederlassungen. Sie schaffen belastbare Kontakte und tragen unsere medizinische Kompetenz in der Nephrologie nach außen. Für klinische Studien identifizieren Sie geeignete Institutionen und beraten Studienärzte, Prüfärzte und Site Manager bei der Durchführung. Darüber hinaus erstellen Sie medizinisch-wissenschaftliche Präsentationen, die Sie vor Fachpublikum persönlich halten, bzw. identifizieren geeignete Referenten. Ihre Aufgaben umfassen: Qualifizierte, kompetente Betreuung und Neugewinnung von externen Experten, Referenten und medizinisch-wissenschaftlichen Zentren Aufbau belastbarer Beziehungen durch persönlichen wissenschaftlichen Informationsaustausch unter Berücksichtigung des jeweiligen medizinischen Plans Aufbau und Pflege von wissenschaftlichem und medizinischem Fachwissen (Indikationen und Produkte) Teilnahme an internationalen, nationalen und regionalen Kongressen und Symposien Konzeption, Budgetierung, Initiierung und Betreuung überregionaler und regionaler wissenschaftlicher Fortbildungsveranstaltungen Bereitstellung wissenschaftlicher Präsentationen und Beantwortung medizinischer Anfragen im Feld Unterstützung interner und externer Studienprojekte Crossfunktionale Zusammenarbeit, u.a. mit dem Vertrieb Entwicklung persönlicher und beruflicher Fähigkeiten zur Verbesserung von Fertigkeiten Sicherstellung der Einhaltung geltender lokaler und globaler Gesetze, Vorschriften, Richtlinien sowie Unternehmensrichtlinien und -verfahren Für diese Rolle sollten Sie folgenden Voraussetzungen mitbringen: Abgeschlossenes naturwissenschaftliches oder medizinisches Studium Erfahrungen in den Bereichen Forschung, pharmazeutisch-medizinische Industrie oder/und klinische Praxis Fähigkeit zur schnellen und selbstständigen Einarbeitung in neue Indikationen und Sachverhalte Sehr gute Kommunikations- und Präsentationstechniken wissenschaftlicher Inhalte Umsetzung medizinischer Strategien Hohe Belastbarkeit in einem dynamischen Arbeits- und Marktumfeld Teamfähigkeit Hohe intrinsische Motivation Selbstständigkeit und hohe persönliche Flexibilität im Aufgabenfeld Reisebereitschaft Sehr gute Deutsch und Englischkenntnisse Erfahrungen in der Nephrologie wünschenswert Wir suchen einen starken Teamplayer mit guten Kommunikations- und Netzwerkfähigkeiten. Wichtige Kompetenzen für diese Rolle sind unternehmerisches Denken und die Fähigkeit, Stakeholder zu beeinflussen und zu überzeugen. About CSL Vifor CSL Vifor aims to become the global leader in iron deficiency and nephrology. The company is a partner of choice for pharmaceuticals and innovative patient-focused solutions across iron, dialysis, nephrology and rare conditions. CSL Vifor strives to help patients around the world with severe, chronic and rare diseases lead better, healthier lives. It specializes in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision patient care. For more information, please visit viforpharma.com We want CSL to reflect the world around us As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL. Do work that matters at CSL Vifor! CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please click here.Über das Unternehmen:1510 Vifor Pharma Deutschland GmbH

Ingenieur Schiffsbau als Technical Manager Dry (m/w/d)Wer wir sindDie HGK Shipping ist das führende Binnenschifffahrtsunternehmen in Europa. Wir sind wegweisender Partner in der Trocken-, Gas- und Chemieschifffahrt. Mit einem Flottenbestand von über 350 eigenen und gecharterten Binnenschiffen befördern wir pro Jahr etwa 43 Mio. Tonnen Fracht. Im Verbund der HGK Gruppe kombinieren wir durch moderne Konzepte die Verkehrsträger Schiene, Wasserwege und Straße zu nachhaltigen Transportketten und sind Teil einer der führenden Akteure im intermodalen Güterverkehr. Mehr als 2500 Menschen arbeiten heute von Rotterdam bis Basel unter dem Dach der HGK-Gruppe.Für unsere Business Unit Ship Management am Standort Duisburgsuchen wir Sie zum frühestmöglichen Zeitpunkt unbefristet in Vollzeit (40 Std.) alsTechnical Superintendent DryIhre Aufgaben * Technische Betreuung von definierten Fahrzeugeinheiten (motorisiert & nicht motorisiert) der Trockengüterschifffahrts-Flotte * Technische Betreuung unserer Umschlag- und Lageranlagen in Kooperation mit Kollegen on- und off-site * Beurteilen des technischen Zustands der Flotte und weiterer Anlagen durch regelmäßige Bord-/Vorortbesuche * Planen, Budgetieren, Durchführen und Überwachen von Wartungs-, Instandhaltungs-, Attest- und Investitionsmaßnahmen * Unterstützung des Manager Fleet bei der Erarbeitung von Ausschreibungsunterlagen sowie der Nachkalkulation von Projekten * Beauftragen, begleiten und überwachen von Dienstleistern und Lieferanten * Unterstützung der kommerziellen und operativen Bereiche bei technischen Fragestellungen * Unterstützung und Zusammenarbeit mit der Abteilung QEHS und ArbeitssicherheitIhr Profil * Sie haben ein abgeschlossenes Studium (B.Sc./Dipl.-Ing.) in der Fachrichtung Schiffbau, Schiffsmaschinenbau oder Schiffstechnik und Sie können erste praktische Erfahrungen vorweisen * alternativ haben Sie langjährige Erfahrung als Schiffsführer und nachweislich Kenntnisse im Bereich der Wartung- und Instandhaltung von schiffstechnischen Anlagen und Maschinen * alternativ haben Sie Erfahrung als Projektmanager an einer Schiffswerft oder einem der Schifffahrt nahen Gewerbezweig * Sie besitzen eine Hands-on-Mentalität und sind flexibel * Sie verfügen über einen sicheren Umgang mit gängigen MS-Office-Anwendungen * Sie haben ein Faible für technische Innovationen und sind aufgeschlossen für Neuerungen * Sie sind teamfähig, überzeugen durch Kommunikationsgeschick auf unterschiedlichen Verantwortungsebenen, sicheres Auftreten und Organisationstalent * Sie sind engagiert, zuverlässig, sorgfältig und schätzen eine selbstständige Arbeitsweise * Deutsch und Englisch beherrschen Sie in Wort und SchriftUnser AngebotWir bieten Ihnen interessante sowie anspruchsvolle Tätigkeiten in einem international wachsenden Unternehmen. Es erwarten Sie ein angenehmes Arbeitsklima in einem sympathischen Team, individuelle Entwicklungs- und Weiterbildungsmöglichkeiten sowie langfristige Perspektiven. Neben einer attraktiven Vergütung bieten wir Ihnen umfangreiche Sozialleistungen.Interesse?Dann freuen wir uns auf Ihre vollständige Bewerbung. Bitte bewerben Sie sich ausschließlich über unser Jobportal unter Angabe Ihrer Gehaltsvorstellung und Verfügbarkeit.Ihre Daten werden für den Bewerbungsprozess elektronisch gespeichert, verarbeitet und genutzt. Nach Abschluss des Bewerbungsprozesses löschen wir Ihre Daten spätestens nach 6 Monaten, sofern Sie keiner weiteren Speicherung zustimmen.HGK Shipping GmbHSarah Mantler / HR Business PartnerTelefon +49 203 3958 7112 Standort HGK Shipping, Krefeld

Technischer Ingenieur als Technical Manager Dry (m/w/d)Wer wir sindDie HGK Shipping ist das führende Binnenschifffahrtsunternehmen in Europa. Wir sind wegweisender Partner in der Trocken-, Gas- und Chemieschifffahrt. Mit einem Flottenbestand von über 350 eigenen und gecharterten Binnenschiffen befördern wir pro Jahr etwa 43 Mio. Tonnen Fracht. Im Verbund der HGK Gruppe kombinieren wir durch moderne Konzepte die Verkehrsträger Schiene, Wasserwege und Straße zu nachhaltigen Transportketten und sind Teil einer der führenden Akteure im intermodalen Güterverkehr. Mehr als 2500 Menschen arbeiten heute von Rotterdam bis Basel unter dem Dach der HGK-Gruppe.Für unsere Business Unit Ship Management am Standort Duisburgsuchen wir Sie zum frühestmöglichen Zeitpunkt unbefristet in Vollzeit (40 Std.) alsTechnical Superintendent DryIhre Aufgaben * Technische Betreuung von definierten Fahrzeugeinheiten (motorisiert & nicht motorisiert) der Trockengüterschifffahrts-Flotte * Technische Betreuung unserer Umschlag- und Lageranlagen in Kooperation mit Kollegen on- und off-site * Beurteilen des technischen Zustands der Flotte und weiterer Anlagen durch regelmäßige Bord-/Vorortbesuche * Planen, Budgetieren, Durchführen und Überwachen von Wartungs-, Instandhaltungs-, Attest- und Investitionsmaßnahmen * Unterstützung des Manager Fleet bei der Erarbeitung von Ausschreibungsunterlagen sowie der Nachkalkulation von Projekten * Beauftragen, begleiten und überwachen von Dienstleistern und Lieferanten * Unterstützung der kommerziellen und operativen Bereiche bei technischen Fragestellungen * Unterstützung und Zusammenarbeit mit der Abteilung QEHS und ArbeitssicherheitIhr Profil * Sie haben ein abgeschlossenes Studium (B.Sc./Dipl.-Ing.) in der Fachrichtung Schiffbau, Schiffsmaschinenbau oder Schiffstechnik und Sie können erste praktische Erfahrungen vorweisen * alternativ haben Sie langjährige Erfahrung als Schiffsführer und nachweislich Kenntnisse im Bereich der Wartung- und Instandhaltung von schiffstechnischen Anlagen und Maschinen * alternativ haben Sie Erfahrung als Projektmanager an einer Schiffswerft oder einem der Schifffahrt nahen Gewerbezweig * Sie besitzen eine Hands-on-Mentalität und sind flexibel * Sie verfügen über einen sicheren Umgang mit gängigen MS-Office-Anwendungen * Sie haben ein Faible für technische Innovationen und sind aufgeschlossen für Neuerungen * Sie sind teamfähig, überzeugen durch Kommunikationsgeschick auf unterschiedlichen Verantwortungsebenen, sicheres Auftreten und Organisationstalent * Sie sind engagiert, zuverlässig, sorgfältig und schätzen eine selbstständige Arbeitsweise * Deutsch und Englisch beherrschen Sie in Wort und SchriftUnser AngebotWir bieten Ihnen interessante sowie anspruchsvolle Tätigkeiten in einem international wachsenden Unternehmen. Es erwarten Sie ein angenehmes Arbeitsklima in einem sympathischen Team, individuelle Entwicklungs- und Weiterbildungsmöglichkeiten sowie langfristige Perspektiven. Neben einer attraktiven Vergütung bieten wir Ihnen umfangreiche Sozialleistungen.Interesse?Dann freuen wir uns auf Ihre vollständige Bewerbung. Bitte bewerben Sie sich ausschließlich über unser Jobportal unter Angabe Ihrer Gehaltsvorstellung und Verfügbarkeit.Ihre Daten werden für den Bewerbungsprozess elektronisch gespeichert, verarbeitet und genutzt. Nach Abschluss des Bewerbungsprozesses löschen wir Ihre Daten spätestens nach 6 Monaten, sofern Sie keiner weiteren Speicherung zustimmen.HGK Shipping GmbHSarah Mantler / HR Business PartnerTelefon +49 203 3958 7112 Standort HGK Shipping, Cologne

Technischer Ingenieur als Technical Manager Dry (m/w/d)Wer wir sindDie HGK Shipping ist das führende Binnenschifffahrtsunternehmen in Europa. Wir sind wegweisender Partner in der Trocken-, Gas- und Chemieschifffahrt. Mit einem Flottenbestand von über 350 eigenen und gecharterten Binnenschiffen befördern wir pro Jahr etwa 43 Mio. Tonnen Fracht. Im Verbund der HGK Gruppe kombinieren wir durch moderne Konzepte die Verkehrsträger Schiene, Wasserwege und Straße zu nachhaltigen Transportketten und sind Teil einer der führenden Akteure im intermodalen Güterverkehr. Mehr als 2500 Menschen arbeiten heute von Rotterdam bis Basel unter dem Dach der HGK-Gruppe.Für unsere Business Unit Ship Management am Standort Duisburgsuchen wir Sie zum frühestmöglichen Zeitpunkt unbefristet in Vollzeit (40 Std.) alsTechnical Superintendent DryIhre Aufgaben * Technische Betreuung von definierten Fahrzeugeinheiten (motorisiert & nicht motorisiert) der Trockengüterschifffahrts-Flotte * Technische Betreuung unserer Umschlag- und Lageranlagen in Kooperation mit Kollegen on- und off-site * Beurteilen des technischen Zustands der Flotte und weiterer Anlagen durch regelmäßige Bord-/Vorortbesuche * Planen, Budgetieren, Durchführen und Überwachen von Wartungs-, Instandhaltungs-, Attest- und Investitionsmaßnahmen * Unterstützung des Manager Fleet bei der Erarbeitung von Ausschreibungsunterlagen sowie der Nachkalkulation von Projekten * Beauftragen, begleiten und überwachen von Dienstleistern und Lieferanten * Unterstützung der kommerziellen und operativen Bereiche bei technischen Fragestellungen * Unterstützung und Zusammenarbeit mit der Abteilung QEHS und ArbeitssicherheitIhr Profil * Sie haben ein abgeschlossenes Studium (B.Sc./Dipl.-Ing.) in der Fachrichtung Schiffbau, Schiffsmaschinenbau oder Schiffstechnik und Sie können erste praktische Erfahrungen vorweisen * alternativ haben Sie langjährige Erfahrung als Schiffsführer und nachweislich Kenntnisse im Bereich der Wartung- und Instandhaltung von schiffstechnischen Anlagen und Maschinen * alternativ haben Sie Erfahrung als Projektmanager an einer Schiffswerft oder einem der Schifffahrt nahen Gewerbezweig * Sie besitzen eine Hands-on-Mentalität und sind flexibel * Sie verfügen über einen sicheren Umgang mit gängigen MS-Office-Anwendungen * Sie haben ein Faible für technische Innovationen und sind aufgeschlossen für Neuerungen * Sie sind teamfähig, überzeugen durch Kommunikationsgeschick auf unterschiedlichen Verantwortungsebenen, sicheres Auftreten und Organisationstalent * Sie sind engagiert, zuverlässig, sorgfältig und schätzen eine selbstständige Arbeitsweise * Deutsch und Englisch beherrschen Sie in Wort und SchriftUnser AngebotWir bieten Ihnen interessante sowie anspruchsvolle Tätigkeiten in einem international wachsenden Unternehmen. Es erwarten Sie ein angenehmes Arbeitsklima in einem sympathischen Team, individuelle Entwicklungs- und Weiterbildungsmöglichkeiten sowie langfristige Perspektiven. Neben einer attraktiven Vergütung bieten wir Ihnen umfangreiche Sozialleistungen.Interesse?Dann freuen wir uns auf Ihre vollständige Bewerbung. Bitte bewerben Sie sich ausschließlich über unser Jobportal unter Angabe Ihrer Gehaltsvorstellung und Verfügbarkeit.Ihre Daten werden für den Bewerbungsprozess elektronisch gespeichert, verarbeitet und genutzt. Nach Abschluss des Bewerbungsprozesses löschen wir Ihre Daten spätestens nach 6 Monaten, sofern Sie keiner weiteren Speicherung zustimmen.HGK Shipping GmbHSarah Mantler / HR Business PartnerTelefon +49 203 3958 7112 Standort HGK Shipping, Wesel

Job Description We are looking for a dedicated, experienced Construction Instrumentation and Control QAQC Manager to join us in our mission to contribute to a greener future. The role is a part of our excellent Construction Quality Site team based in Skellefteå (Sweden). By joining us, you will be a key player in establishing a sound QAQC Site team and will contribute to building one of the first large scale European battery factories. About the jobBe an Instrumentation and Control focal Point for QAQC matters for site projects, and facilities development. Responsible for developing implementing, auditing and monitoring project QAQC Plan and programs in compliance Company Specifications, applicable International Codes and Standards, and local Swedish Standards will be also a plus. Ensure that plants and factory facilities are constructed according to Company and Project Specifications, design documents, applicable codes and standards and acceptable work practices.About the teamJoin us to work into an international environment team of more than 151 nationalities, based in the north of Sweden, where an active QAQC team is rapidly growing to achieve great goals set for 2025. The candidate will contribute to the implementation of a QAQC system along with his team, amongst all site contractors and subcontractors to turn green battery factory in a tangible reality. Key responsibilities include but are not limited to:Develop and maintain Project Quality Plans for the different projectsSet up and develop QAQC procedures, ITP, quality management systems to effectively monitor QAQC performance, review and approve ITP's, ITR'S and all formal documentation, report KPI, support project activities with EPC contractorsWorking alongside Swedish personnel and understanding the Swedish codes of practiceEnsuring quality assurance of all work scopes is maintained and all work is performed in accordance with company policies and the Health & Safety at work actTo coordinate the establishment, implementation and, maintenance of the Project inspection and test programs and associated witness point(s) time schedule on a system-by-system basisTakes the lead on resolving all Non-conformance Reports (NCR’s) and Corrective Action Requests (CARs), with an emphasis on investigating root cause analysis, identifying trends, and driving improvementsPersonal success factors:The person we are looking for is driven, caring and structuredYou thrive by leading others and work towards common goalsYou are used to a high paced work environment and got good time management skillsQualities that we cherish are flexibility, sense of quality, friendliness, motivation to take on new challenges, grit and a sense of humourNorthvolt is an equal opportunity employer. We're a diverse group of individuals, united by a common mission, who recognise that while our actions as individuals have a role to play in driving Northvolt towards its goals, we always seek to move forward as a team. We offer you an open and welcoming atmosphere where we win as a team – and fail as a team. Northvolt is growing at the speed of light and we are a strong believer in internal career development. For us it’s important to look at your skills and potential, please refrain form including your picture and age with your application to help us with this.Apply with CV in English or your complete LinkedIn profile. Full time employment, fixed salary. Planned starting date is ASAP.

Company DescriptionWorking at Boskalis is about creating new horizons and sustainable solutions. In a world where population growth, an increase of global trade, demand for (renewable) energy and climate change are driving forces, we challenge you to make your mark in finding innovative and relevant solutions for complex infrastructural and marine projects.Dredging, Explosive Ordnance Disposal Services Offshore and Military Ordnance Removal Onshore - the specialists at Heinrich Hirdes always use and develop further the latest technology. Through the group of companies an enormous amount of know-how is available to us for very different challenges.Job DescriptionMake your mark as SHE-Q Manager at Boskalis!As SHEQ -Manager within Hirdes Boskalis, you can make your mark across our three business units by ensuring proper execution and maintenance of SHEQ policies, programs and management systems on our vessels and projects, in order to comply with company / industry standards and German legislation. You are open to new experiences, willing to learn and take responsibility. This position might be just the right challenge for you!Your responsibilities as SHE-Q ManagerActively supporting the organization on SHEQ related matters and monitoring SHEQ training/familiarization.Achieving results by understanding the added value of our SHEQ role for the business: providing SHEQ knowledge, documentation and deliverables like Risk Management Support (contributing to Risk Assessments, Job Hazard Analyses, revision of Assessments and Analyses).Providing feedback, report and advise management to increase SHEQ knowledge and awareness by initiating and organizing training, assessments, client audits, internal audits and sub-contractor audits.Analyzing and assessing processes for the benefit of complying to SHEQ policies and programs. Analyzing, assessing and continuously improving corrective measures. Keep relevant colleagues engaged in improvement processes.Coaching, facilitating the process and organising training on-the-job and directing of reports.Leading the local SHE-Q team and liaising with the Group SHE-Q team.Your qualities and experience You can move ahead as an SHE-Q Manager if you have:SHEQ education on bachelor level (e.g. SIFA, Quality Management, Auditing).In-depth knowledge of German legislation.A good command of written and spoken English and German is a must.You’re willing to travel (within Europe) on a fairly regular basis. QualificationsWhat you can expect A dynamic environment: A job where you can make an impact, in an earth-moving company, as part of a diverse, international team of experts.Rewarding conditions:A competitive salary and much more, including holiday allowance, travel allowance, leased or shared car.Career development: Plenty of opportunities to realize your full potential. Challenge yourself with (online) courses in our Boskalis academy.Additional Information Where you will work: Place of work is Hamburg. Regular site visits are part of the job. The possibility of working from home on a daily basis is given in accordance with your manager.Full/part-time job: The position of SHE-Q Manager is a full-time (40 hours a week) job.Next steps: Apply easily by completing the online application form. Interviews are held online and in the office. Once it’s clear we’re a good match, we’ll make you an offer – and look forward to welcoming you to the company.Über das Unternehmen:Boskalis

Clinical Research Associate / Klinischer Monitor / Site Manager (m/w/d) - homebased (Region Nord- oder Ostdeutschland) bei Alcedis GmbH | softgarden Clinical Research Associate / Klinischer Monitor / Site Manager (m/w/d) - homebased (Region Nord- oder Ostdeutschland) Vollzeit Gießen, Deutschland Remote Mit Berufserfahrung 07.02.24 Als Clinical Research Associate / Klinischer Monitor / Site Manager (m/w/d) - homebased (Region Nord- oder Ostdeutschland) - unterstützt du unsere Fachabteilung Clinical Operations beim Überwachen und Sicherstellen von Qualitätsmerkmalen in Gesundheitszentren vor Ort sowie bei der erfolgreichen Planung und Durchführung von Klinischen Arzneimittelprüfungen der Phasen I-IV, nicht-interventionellen Studien sowie Medizinprodukte-Studien. Du betreust eigenständig die entsprechende Region und wirst für eine optimale Einbindung in die Prozesse bei Alcedis 1-2 Tage im Quartal in Gießen (Hessen) eingesetzt. Was du bei uns tustOversight-Tätigkeiten/ Lead-Site-Management in nationalen und internationalen Projekten (z.B. Training des CRA-Teams, Review von Monitoring Reports, Koordination der Besuche und der regelmäßigen Kontakte zu den Zentren, Kontakt zum Sponsor bzgl. Monitoring/ Site Management) Klassische CRA-Tätigkeiten in Abhängigkeit der Projekte: Unterstützung bei der Organisation der Studie in den Prüfzentren und Betreuung der PrüfärzteVorbereitung, Durchführung und Nachbereitung von Initiierungs-, Monitor- und Abschlussbesuchen (On-site oder Remote/Online) inkl. BerichterstellungAbfrage des Studienstands in den Prüfzentren (nach vorgegebenem Leitfaden) sowie DokumentationValidierung der von den Prüfärzten erhobenen Studien-Daten (Quelldatenvergleich)Überprüfung der Prüfzentren auf Einhaltung der geltenden Richtlinien und GesetzeAbstimmung mit Datenmanager und ProjektleiterErstellung von Queries (Rückfragen) und Überwachung des Query-ProzessSchulung der Prüfärzte und Dokumentare auf EDC-SoftwareDurchführbarkeitsprüfung (Feasibility) für neue Projekte mit PrüfzentrenUnterstützung bei der Erstellung von Studienunterlagen inkl. Versand und TrackingVorbereitung von Unterlagen zur Einreichung bei Behörden und EthikkommissionenBegleitung von Audits/Inspektionen in den PrüfzentrenAdministrative Unterstützung der Teamleitung:Erstellung und Updates von SOPsEinarbeitung und Coaching von Junior-CRAsCo-Monitoring zur QualitätsüberprüfungMitwirkung bei der Überarbeitung des elektronischen Reporting-SystemsMonitoring-Konzepterstellung für Kunden auf Anfrage Wer du bistDu hast ein abgeschlossenes Studium aus dem Bereich der Naturwissenschaften oder Life Sciences, bzw. besitzt eine Study Nurse oder vergleichbare QualifikationBerufserfahrung (>2 Jahre) in der Durchführung GCP-konformer klinischer Studien innerhalb der Industrie (z.B. CRO, Pharma oder Biotech) ist verpflichtendDu arbeitest selbständig und vorausschauend bei Planung und UmsetzungDu besitzt eine hohe Sozialkompetenz und eine ausgeprägte Teamfähigkeit Du besitzt sehr gute Kommunikations- und OrganisationskompetenzenExzellente Deutschkenntnisse setzen wir vorausDeine Kenntnisse in Englisch (Wort und Schrift) sind sehr gutDu arbeitest gerne mit elektronischen Daten und Datenbanken und bringst gute Kenntnisse in den Office-Anwendungen mitDu besitzt Reisebereitschaft und Flexibilität Warum du dich für uns entscheidestWir leisten jeden Tag einen bedeutsamen Beitrag zum medizinischen Fortschritt - bei uns findest du eine Stelle, die nicht nur sinnstiftend ist, sondern auch deinem Purpose entspricht und ihn fördertDie fachliche Übereinstimmung ist wichtig, mindestens genauso viel zählen für uns aber auch eine angenehme Arbeitsatmosphäre, kollegialer Zusammenhalt und die Passung ins Team! Wir leben eine moderne und offene Unternehmenskultur mit flachen Hierarchien, ohne Dresscode und alle per Du – gerne auch schon im Bewerbungsverfahren Du findest in einem international erfolgreichen und stetig wachsenden Unternehmen ein zukunftsorientiertes und sicheres Arbeitsumfeld vor. Unser Fokus liegt auf langfristigen und vertrauensvollen MitarbeiterbeziehungenUnsere Vergütungsstruktur ist leistungsbezogen dynamisch gestaltet und bietet dir kontinuierliche EntwicklungsmöglichkeitenWir bieten 30 Urlaubstage bei einer 5-Tage-Woche, flexible Arbeitszeiten und ermöglichen dir im Rahmen einer homebased-Stelle die Option, von zuhause aus zu arbeitenNeben den kleinen Extras wie Obstkorb, Getränkeflatrate und Tischkicker bieten wir dir weitere attraktive Benefits, darunter Gesundheitsförderungsmaßnahmen, Job-Fahrrad, VWL-Zahlung, regelmäßige Firmenveranstaltungen und Teambuilding-Aktivitäten, wechselnde exklusive Mitarbeiter-Angebote und vieles mehr Deine BewerbungBereit für deinen neuen Job? Dann mache jetzt den nächsten Schritt - wir freuen uns über deine Bewerbung!Kontakt:Human Resources: Carolin Gerhard, Alcedis GmbH, Winchesterstr. 3, 35394 Gießen, 0641/ 94436-0 Standort Alcedis GmbH, Giessen

Req ID:416175 At Alstom, we understand transport networks and what moves people. From high-speed trains, metros, monorails, and trams, to turnkey systems, services, infrastructure, signalling and digital mobility, we offer our diverse customers the broadest portfolio in the industry. Every day, more than 80 000 colleagues lead the way to greener and smarter mobility worldwide, connecting cities as we reduce carbon and replace cars. Could you be the full-time EHS Manager (f/m/d), based in Goerlitz we’re looking for? Your future role Take on a new challenge and apply your expertise in a new cutting-edge field. You’ll report to the Site Managing Director in Görlitz and work alongside passionate, motivated and dedicated teammates.You'll be the person to push EHS action implementation forward. No two days are the same, but day-to-day, you will lead a by example and advise, help, coach and support the operational management in the EHS actions implementation to reach Alstom EHS objectives. Prepare the local yearly EHS plan consistent with Alstom Transport strategy and objectives. Mobilize and coordinate with others to meet those objectives and deploy the plan. We’ll look to you for:• Support Site Management in achieving EHS resultsDrive the implementation of EHS policy and the improvement of EHS results in the site.Ensure EHS Risk Assessment is done & appropriate measures to control risks are defined for the Site.Prepare, implement and maintain emergency plans at Site level. • Lead the EHS function and Develop Site EHS Management System in the siteMonitor, assist, coach, assess, develop the EHS teams in the site.Involve social and medical partners and communicate with them about EHS.Develop, deploy and maintain the local procedures and tools applicable to the Site.Ensure that Alstom EHS standards and tools (AZDP, TOP_E, Transport Key processes) are deployed at Site level.Budget resposibility for EHS.Monitor compliance with all relevant statutory, regulatory, contractual and company requirements & propose actions to correct any gap. • Develop EHS culture in the siteInfluence the site EHS performance, facilitate change and EHS continuous improvement.Built the site EHS communication plan.Prepare and implement an EHS training plan and program with the support from HR. • Report, Measure & ReviewEnsure that Accidents/Incidents are first prevented, and when occurring, reported, recorded, investigated and analyzed.Prepare and submit monthly EHS reports. Feed EHS Teranga reporting system in line with Group reporting requirements. Organize and lead internal EHS audits and inspections of the EHS reporting process.All about you We value passion and attitude over experience. That’s why we don’t expect you to have every single skill. Instead, we’ve listed some that we think will help you succeed and grow in this role: • Master Degree in Engineering or equivalent with EHS backround. • You have successfully completed a technical degree with the qualification to the occupational safety specialist. • Relevant experience in a previous role, within the manufacturing industry. • Structured working method, result and process-oriented. • Fluent English and German language skills. • Demonstrated proficiency in Microsoft office. • Team oriented and excellent communication skills are essential. • You are willing to learn and be open-minded. Things you’ll enjoy Join us on a life-long transformative journey – the rail industry is here to stay, so you can grow and develop new skills and experiences throughout your career. You’ll also: • Enjoy stability, challenges and a long-term career progression, free from boring daily routines. • Collaborate with transverse teams and helpful colleagues. • Contribute to innovative projects. • Steer your career in whatever direction you choose across functions and countries. • Benefit from our investment in your development, through award-winning learning. • Benefit from a fair and dynamic reward package that recognises your performance and potential, plus comprehensive and competitive social coverage (life, medical, pension). You don’t need to be a train enthusiast to thrive with us. We guarantee that when you step onto one of our trains with your friends or family, you’ll be proud. If you’re up for the challenge, we’d love to hear from you! Important to noteAs a global business, we’re an equal-opportunity employer that celebrates diversity across the 63 countries we operate in. We’re committed to creating an inclusive workplace for everyone. Job Type:​Experienced​Über das Unternehmen:AlstomBranche:Manager, Management

Als Clinical Research Associate / Klinischer Monitor / Site Manager (m/w/d) - homebased (Region Nord- oder Ostdeutschland) - unterstützt du unsere Fachabteilung Clinical Operations beim Überwachen und Sicherstellen von Qualitätsmerkmalen in Gesundheitszentren vor Ort sowie bei der erfolgreichen Planung und Durchführung von Klinischen Arzneimittelprüfungen der Phasen I-IV, nicht-interventionellen Studien sowie Medizinprodukte-Studien. Du betreust eigenständig die entsprechende Region und wirst für eine optimale Einbindung in die Prozesse bei Alcedis 1-2 Tage im Quartal in Gießen (Hessen) eingesetzt. Was du bei uns tustOversight-Tätigkeiten/ Lead-Site-Management in nationalen und internationalen Projekten (z.B. Training des CRA-Teams, Review von Monitoring Reports, Koordination der Besuche und der regelmäßigen Kontakte zu den Zentren, Kontakt zum Sponsor bzgl. Monitoring/ Site Management) Klassische CRA-Tätigkeiten in Abhängigkeit der Projekte: Unterstützung bei der Organisation der Studie in den Prüfzentren und Betreuung der PrüfärzteVorbereitung, Durchführung und Nachbereitung von Initiierungs-, Monitor- und Abschlussbesuchen (On-site oder Remote/Online) inkl. BerichterstellungAbfrage des Studienstands in den Prüfzentren (nach vorgegebenem Leitfaden) sowie DokumentationValidierung der von den Prüfärzten erhobenen Studien-Daten (Quelldatenvergleich)Überprüfung der Prüfzentren auf Einhaltung der geltenden Richtlinien und GesetzeAbstimmung mit Datenmanager und ProjektleiterErstellung von Queries (Rückfragen) und Überwachung des Query-ProzessSchulung der Prüfärzte und Dokumentare auf EDC-SoftwareDurchführbarkeitsprüfung (Feasibility) für neue Projekte mit PrüfzentrenUnterstützung bei der Erstellung von Studienunterlagen inkl. Versand und TrackingVorbereitung von Unterlagen zur Einreichung bei Behörden und EthikkommissionenBegleitung von Audits/Inspektionen in den PrüfzentrenAdministrative Unterstützung der Teamleitung:Erstellung und Updates von SOPsEinarbeitung und Coaching von Junior-CRAsCo-Monitoring zur QualitätsüberprüfungMitwirkung bei der Überarbeitung des elektronischen Reporting-SystemsMonitoring-Konzepterstellung für Kunden auf Anfrage Wer du bistDu hast ein abgeschlossenes Studium aus dem Bereich der Naturwissenschaften oder Life Sciences, bzw. besitzt eine Study Nurse oder vergleichbare QualifikationBerufserfahrung (>2 Jahre) in der Durchführung GCP-konformer klinischer Studien innerhalb der Industrie (z.B. CRO, Pharma oder Biotech) ist verpflichtendDu arbeitest selbständig und vorausschauend bei Planung und UmsetzungDu besitzt eine hohe Sozialkompetenz und eine ausgeprägte Teamfähigkeit Du besitzt sehr gute Kommunikations- und OrganisationskompetenzenExzellente Deutschkenntnisse setzen wir vorausDeine Kenntnisse in Englisch (Wort und Schrift) sind sehr gutDu arbeitest gerne mit elektronischen Daten und Datenbanken und bringst gute Kenntnisse in den Office-Anwendungen mitDu besitzt Reisebereitschaft und Flexibilität Warum du dich für uns entscheidestWir leisten jeden Tag einen bedeutsamen Beitrag zum medizinischen Fortschritt - bei uns findest du eine Stelle, die nicht nur sinnstiftend ist, sondern auch deinem Purpose entspricht und ihn fördertDie fachliche Übereinstimmung ist wichtig, mindestens genauso viel zählen für uns aber auch eine angenehme Arbeitsatmosphäre, kollegialer Zusammenhalt und die Passung ins Team! Wir leben eine moderne und offene Unternehmenskultur mit flachen Hierarchien, ohne Dresscode und alle per Du – gerne auch schon im Bewerbungsverfahren Du findest in einem international erfolgreichen und stetig wachsenden Unternehmen ein zukunftsorientiertes und sicheres Arbeitsumfeld vor. Unser Fokus liegt auf langfristigen und vertrauensvollen MitarbeiterbeziehungenUnsere Vergütungsstruktur ist leistungsbezogen dynamisch gestaltet und bietet dir kontinuierliche EntwicklungsmöglichkeitenWir bieten 30 Urlaubstage bei einer 5-Tage-Woche, flexible Arbeitszeiten und ermöglichen dir im Rahmen einer homebased-Stelle die Option, von zuhause aus zu arbeitenNeben den kleinen Extras wie Obstkorb, Getränkeflatrate und Tischkicker bieten wir dir weitere attraktive Benefits, darunter Gesundheitsförderungsmaßnahmen, Job-Fahrrad, VWL-Zahlung, regelmäßige Firmenveranstaltungen und Teambuilding-Aktivitäten, wechselnde exklusive Mitarbeiter-Angebote und vieles mehr Deine BewerbungBereit für deinen neuen Job? Dann mache jetzt den nächsten Schritt - wir freuen uns über deine Bewerbung!Kontakt:Human Resources: Carolin Gerhard, Alcedis GmbH, Winchesterstr. 3, 35394 Gießen, 0641/ 94436-0Über das Unternehmen:Alcedis GmbH

About Us Yuneec has pushed the limits above and beyond in electric aviation for over 20 years. From the first commercially successful ready-to-fly fixed wing RC airplane, to ground-breaking electric aircraft and drone systems for commercial use. We offer a diverse selection of drone models for a wide range of commercial applications - from a drone with a thermal camera to help you identify extinguish fire hotspots faster to a drone with an inspection camera to fly at a greater distance from an object.Yuneec manufactures over one million units a year that accommodate a range of customers with offices in North America, Europe and Asia. Yuneec embraces innovation, making aerial photography and data capture attainable at any level of flight experience. Our UAVs are the perfect solution for long flight times and a proven and robust technology in an all-in-one package. It's built for inspection, law enforcement, security, construction, surveying, and mapping applications in addition to offering cinematic imaging payload systems.To find more about Yuneec EU and our Products : www.yuneec.comAbout The JobWe are seeking an Sales Manager to reinforce our team in any city in Germany. We offer a flexible attendance mode, such as telecommuting, you will just be responsible for sales results, report regularly to head office on site in Kaltenkirchen. Responsibilities: Develop market, potential customers and tap potential demand into orders. Maintain existing customers and keep good relationships, follow-up needs. Collect industry information, grasp market dynamics. Support and cooperate with service team. Being responsible.for other duties which may be delegated.Requirements: Interested in UVA and Intelligent product. Command of English and German language. Proven writing, active-listening skills, along with outstanding presentation skills. Strong interpersonal and communication skills. Knowledge of advertising and sales promotion techniques. Willing to accept short-term business trip or visit current and potential clients. Good technical knowledge, We Provide:l A flexible work life such as telecommuting + Report to head office regularly.l Competitive base salary and commission, and generous benefits.l Perfect after-sales service and technical team support.l Nice and professional team.l Science and technology change the world. Join us. CV Delivery Channels: Email to E-Mail anzeigen to connect Ms. Jay Wang. We are looking forward to your application. Standort Yuneec Europe GmbH, Hamburg