Überblick über die Statistik des Gehaltsniveaus für "Project Administrator 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 II, 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 Clinical Project Manager II, you will be responsible for managing the clinical projects and ensuring the quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines, and other applicable regulations.                                Join our team and help us deliver clinical trials that will improve patients' lives.        Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projectsManage all project-specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team membersKeep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assignedKnowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areasAssure the proper timelines of the assigned projectsManage the budget for the projectMonitor the workload and the performance of the project teamPlan and monitor the tasks of the team in the specific areasCoordinate the Clinical Research Associates and Clinical Monitors activityCollaborate with Clinical Trial Administrators and Clinical Research Associates in terms of local authorities' approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activitiesAssist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDeliver project-specific trainingOrganise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetingsProvide project updates to the Sponsor, Senior Project Manager, and Project Director/Leader as requiredInform the Project Director/Leader about any issuesPerform co-monitoring visits for the assigned clinical projects as necessaryAct as a tutor for Project Coordinators and Project Managers IMaintain relationships with the Sponsor, including providing project updatesPrepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying with enforcing Company procedures Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similarExcellent 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

Location: Germany- 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 II, to join their clinical operations team in Germany. 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 Clinical Project Manager II, you will be responsible for managing the clinical projects and ensuring the quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines, and other applicable regulations.                                Join our team and help us deliver clinical trials that will improve patients' lives.        Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projectsManage all project-specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team membersKeep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assignedKnowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areasAssure the proper timelines of the assigned projectsManage the budget for the projectMonitor the workload and the performance of the project teamPlan and monitor the tasks of the team in the specific areasCoordinate the Clinical Research Associates and Clinical Monitors activityCollaborate with Clinical Trial Administrators and Clinical Research Associates in terms of local authorities' approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activitiesAssist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDeliver project-specific trainingOrganise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetingsProvide project updates to the Sponsor, Senior Project Manager, and Project Director/Leader as requiredInform the Project Director/Leader about any issuesPerform co-monitoring visits for the assigned clinical projects as necessaryAct as a tutor for Project Coordinators and Project Managers IMaintain relationships with the Sponsor, including providing project updatesPrepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying with enforcing Company procedures Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similarExcellent 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: GermanyShare: LinkedIn Facebook Twitter Email

Location: Spain - 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 II, to join their clinical operations team in Spain. 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 Clinical Project Manager II, you will be responsible for managing the clinical projects and ensuring the quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines, and other applicable regulations.                                    Join our team and help us deliver clinical trials that will improve patients' lives.            Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projectsManage all project-specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team membersKeep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assignedKnowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areasAssure the proper timelines of the assigned projectsManage the budget for the projectMonitor the workload and the performance of the project teamPlan and monitor the tasks of the team in the specific areasCoordinate the Clinical Research Associates and Clinical Monitors activityCollaborate with Clinical Trial Administrators and Clinical Research Associates in terms of local authorities' approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activitiesAssist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDeliver project-specific trainingOrganise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetingsProvide project updates to the Sponsor, Senior Project Manager, and Project Director/Leader as requiredInform the Project Director/Leader about any issuesPerform co-monitoring visits for the assigned clinical projects as necessaryAct as a tutor for Project Coordinators and Project Managers IMaintain relationships with the Sponsor, including providing project updatesPrepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying with enforcing Company procedures Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similarExcellent 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: SpainShare: LinkedIn Facebook Twitter Email

Location: Germany- 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 Senior Clinical Project Manager,  You will be working on projects from our varied client base, ranging from small to mid-sized pharma, biotech, and medical device companies.       As a Senior Clinical Project Manager, you will be responsible for managing the clinical projects and ensuring the quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines, and other applicable regulations.                         Join our team and help us deliver clinical trials that will improve patients' lives.        Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projectsManage all project-specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team membersKeep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assignedKnowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areasAssure the proper timelines of the assigned projectsManage the budget for the projectMonitor the workload and the performance of the project teamPlan and monitor the tasks of the team in the specific areasCoordinate the Clinical Research Associates and Clinical Monitors activityCollaborate with the Clinical Trial Administrators and Clinical Research Associates in terms of local authorities' approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activitiesAssist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDelivering  project specific trainingsOrganise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetingsProvide project updates to the Sponsor, Senior Project Manager,  and Project Director/Leader as requiredInform the Project Director/Leader about any issuesPerform co-monitoring visits for the assigned clinical projects as necessaryAct as a tutor for Project Coordinators and Project Managers IMaintain relationships with the Sponsor, including providing project updatesPrepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying with and enforcing Company procedures Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similarExcellent 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 @ 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, Project Management, Study ManagementLocation: GermanyShare: LinkedIn Facebook Twitter Email

Location: Netherlands - 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 internal team in Netherlands. This role is a full-time permanent opportunity. 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 managing the clinical projects ensuring quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines and other applicable regulations.                         Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projects.Manage all project specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team members.Keep professionally abreast of all scientific, regulatory and operational aspects relevant to the clinical projects assigned.Knowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areas.Assure the proper timelines of the assigned projects.Manage the budget for the project.Monitor the workload and the performance of the project team.Plan and monitor the tasks of the team in the specific areas.Coordinate the Clinical Research Associates and Clinical Monitors activity.Collaborate with he Clinical Trial Administrators and Clinical Research Associates in terms of local authorities approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activities.Assist the Medical Monitor in preparing protocols, Case Report Forms and final Clinical Study ReportsDeliver project specific trainings.Organise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetings.Provide project updates to the Sponsor, Senior Project Manager and Project Director/Leader as required.Inform the Project Director/Leader about any issues.Perform co-monitoring visits for the assigned clinical projects as necessary.Act as a tutor for Project Coordinators and Project Manager IMaintain relationships with the Sponsor, including providing project updates.Prepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying and enforcing Company procedures. Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similar.Excellent 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 Netherlands:Competitive SalaryGroup health insuranceGreat pension scheme24 vacation daysInternet reimbursementCompany Car with fuel card depending on the function.Dedicated Line Manager The Application Process         Once you have submitted your CV, you will receive an acknowledgement email. If you have the requirements we need, you will be invited for phone interview as the first step. If you would like to discuss the role before applying through the website @

Location: Belgium - 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 internal team in Belgium. This role is a full-time permanent opportunity. 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 managing the clinical projects ensuring quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines and other applicable regulations.                             Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projects.Manage all project specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team members.Keep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assigned.Knowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areas.Assure the proper timelines of the assigned projects.Manage the budget for the project.Monitor the workload and the performance of the project team.Plan and monitor the tasks of the team in the specific areas.Coordinate the Clinical Research Associates and Clinical Monitors activity.Collaborate with he Clinical Trial Administrators and Clinical Research Associates in terms of local authorities approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activities.Assist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDeliver project specific trainings.Organise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetings.Provide project updates to the Sponsor, Senior Project Manager and Project Director/Leader as required.Inform the Project Director/Leader about any issues.Perform co-monitoring visits for the assigned clinical projects as necessary.Act as a tutor for Project Coordinators and Project Manager IMaintain relationships with the Sponsor, including providing project updates.Prepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying and enforcing Company procedures. Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similar.Excellent 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 Belgium:Competitive SalaryGroup and hospitalisation insuranceElectronic meal vouchersInternet reimbursement The Application Process           Once you have submitted your CV, you will receive an acknowledgement email. If you have the requirements we need, you will be invited for 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 send an mail to: [email protected] for more information.                     Who will you be working for?                                            About CROMSOURCE                           CROMSOURCE is a family owned international, full-service Contract Research Organisation who, 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 on 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. The continuous training keeps the resources qualified in terms of competence and expertise and gives to 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.                                                         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 OrganisationSkills: Clinical Project Manager, Clinical Study Manager, Clinical Trial Manager, Senior Clinical Project Manager, clinical trials, CRO, Medical Devices, Study ManagementLocation: BelgiumShare: LinkedIn Facebook Twitter Email

Job Description We are looking for a dedicated Senior Contracts Administrator to join us in our mission to contribute to a greener future. The role is a part of our excellent CAM Program team based in Skellefteå. By joining us, you will be a key player in ramping up and contribute to building one of the first large scale European battery factories. About the jobAs the Senior Contracts Administrator within the CAM business, you will be part of the CAM Program delivery team. Providing oversight, guidance, and management to our construction contractors. Ensuring the interests of Northvolt are protected both financially, reputationally, and professionally. You will be responsible for the successful management for your allocated scope working with other members of the Program team to deliver your contracts efficiently, effectively and in line with the US1 project schedule. Key responsibilities include but are not limited to:Oversight, management, formation and administration of the US1 construction contracts. This includes contract formation and contract administration support during the construction phase.Working with and gaining stakeholder alignment and support from the US1 project team team, during the tender development. tendering, evaluation and award phases so as to be able to secure approvals to award from Northvolt Sourcing Councils. This includes all necessary internal stakeholder management within the project, CAM business and within the broader Northvolt procurement community.Set up new projects in conjunction with the US1 project team to ensure the contract can be administered as per the contract deliverables and requirements. Ensure the necessary work processes are in place to allow the contract to be executed as planned.Supporting the US1 project team with management of change, change orders and variations; and ensuring the US1 project can robustly justify these to Northvolt management.Attendance at monthly contractor meetings as the Northvolt representative.Review and control the monthly invoicing – including the review and approval of payment applications and invoices and tracking progress through to actual payment.Review and approval of all documentation requiring a Northvolt signature in line with the delegation of authority.Participate in Risk & Contingency management and mitigation of any claims during construction.Monitoring and appraising the performance of Contractors and Consultants.Contract closeout in line with accepted practice and Northvolt requirements.Proactive approach with the US1 contractors to avoid Construction Claims and the handling of Claims if they arise.Ensure the values of Northvolt in terms of safety performance are understood and respected.The person we are looking for is flexible, curios and eager to learn. You will get the chance to have a real impact on our success story in Sweden (to start with) and see the results of your work. Our organization values great self-discipline and a natural talent to make things happen. Qualities that we cherish are sense of quality, friendliness, grit and a sense of humor. Northvolt 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.

11-2024 IT Network Administrator (m/f/d) At the Hessian Police Headquarters Deployment (HPE) in Mainz-Kastel in the Central Services Department, in the main subject area Z2 - Information and Communication Technology, subject area Z25, Networks/Multimedia - two permanent full-time positions (40 hours / week) are available at the earliest possible date as IT Network Administrator (m/f/d) Reference number 11-2024 to be filled. As a member of our team, you will become part of the Hessian police force and make an indispensable contribution to safety and quality of life in Hesse. Your work actively contributes to ensuring the police's ability to work and to optimizing it for the future. Our offer A permanent position in the public sector that offers you long-term career security and prospects Varied tasks in an exciting and sometimes unique working environment Versatile and multi-faceted activities and projects Assumption of independent fields of activity according to personal aptitude Job-related, regular training and further education offers Compatibility of family and career: Awarded the \"Family-friendly employer of the state of Hesse\" seal of approval, including a company contingent for the \"wi&you - Schöne Ferien\" vacation program of the city of Wiesbaden Work-life balance: up to 30 days' vacation, overtime compensation in the form of time off, 24 and 31 December off, 1 additional individually plannable day off per year Flexible working hours as part of our service hours with flexitime and digital time recording as well as the option to work from home up to two days a week An attractive salary depending on qualifications and experience up to E11 TV-H plus additional benefits in the form of a child allowance, annual bonus, capital-forming benefits and company pension scheme Free travel with the state ticket for free use of public transport in Hesse and in several neighboring areas, such as Mainz, initially limited until 31.12.2026 Health and sports offers at the place of employment including the right to use the Gympass service An attractive location with good infrastructure and transport links in the state capital of Wiesbaden with direct proximity to the banks of the Rhine as well as a gym and fitness room Free use of the electric charging stations subject to availability Personal business smartphone The chance to develop your career in a dynamic and future-proof environment where there will be many opportunities for personal and professional development in the coming years Your tasks Full support of the authority's networks (commissioning, configuration, administration, development, support and troubleshooting) Planning and implementation/commissioning of new installations, renewals and network expansions Setting up network services, user and device management via Active Directory, certificates, VPN, servers, virtualization Development of demand-oriented standards in the field of multimedia and signal transmission Support for special computing systems (e.g. image processing PCs) Collaboration in subject-specific project groups - also in a leading role Technical guidance of the decentralized field offices Collaboration in the supervision of trainees Your profile Completed vocational training as an IT specialist (m/f/d) for system integration, Bachelor of Computer Science or in a comparable course of study or comparable relevant vocational training in the IT sector Proven knowledge and/or experience in one or more of the following areas: o Network technologies and network administration, ideally with certifications in sub-areas o Configuration and operation of firewalls o Administration, operation and further development of Linux and Windows server landscapes o Virtualization (e.g. vSphere, Proxmox) o Working with ticket systems o UPS systems Ability to organize independently, structured way of working, professional documentation, ability to work in a team and reliability Good written and spoken German (level B2) Driving license class B Also desirable are o Knowledge in the field of multimedia installations and media control (e.g. Crestron, AMX) o Experience in (IT) project management o Knowledge in the field of applied IT security o Trainer aptitude certificate AdA If you would like to contribute your expertise and passion for network technology to strengthen the digital infrastructure of the Hessian police and thus make an important contribution to the security of our country, then apply to us now! Contact: For technical questions, please contact Mr. Spangenberg (Tel. 06134 / 602 - 2250) and Mr. Kerz (Tel. 06134 / 602 - 2255) or send an e-mail to [email protected] . If you have any questions about the selection procedure, please contact Mr. Chada (Tel. 06134 / 602 - 4333). What else is important: A prerequisite for working at the Hessian Police Headquarters is the willingness to participate in a background check for the protection of state institutions and events in accordance with u00a7 13 a of the Hessian Law on Public Safety and Order (HSOG). For this purpose, the attachment \"Declaration of background check\" (in the application portal below the text of the advertisement or under the \"Attachments\" tab) must be completed and uploaded immediately to your applicant profile together with a current identification document (copy of ID card or passport on both sides). General information: The following documents are required for the selection procedure Cover letter Curriculum vitae in tabular form Examination certificate from the apprenticeship or course of study Employment references In the case of foreign qualifications and documents, also the German recognition or translation of the documents in German Certificates of attendance for further education and training courses Proof of a class \"B\" driving license (old: class 3) If applicable, proof of required German language skills (certificate) Proof of valid residence permit and work permit, if applicable Proof of disability/severe disability, if applicable Declaration of background check (with a copy of a valid ID document on both sides) Please send us your detailed application by 20.06.2024 at the latest, preferably via stellensuche.hessen.de or by email to [email protected] . Late applications will not be considered. Unsuccessful applicants will be notified after the selection process has been completed. Only applications that include all required documents can be considered. Employees of the Hessian State Administration are requested to apply via the service portal and, in addition to submitting the complete application documents, to declare their consent to the personnel administration of the Hessian Police Headquarters Operations inspecting their personnel file. To do this, you must complete the attachment \"Declaration of consent to access PA\" (in the application portal below the text of the advertisement or under the \"Attachments\" tab) and upload it to your applicant profile. According to the Hessian Equal Opportunities Act, the local authority is obliged to increase the proportion of women. Applications from women are therefore particularly welcome. Part-time employment is possible in principle, but it must be ensured that the position is filled in full. The Hessian Police Headquarters promotes equality between women and men and supports the compatibility of family and career within the scope of official possibilities and is certified with the seal of approval \"Family-friendly employer state of Hesse\". Volunteering is encouraged in Hesse. Experience and skills acquired in voluntary work can be positively taken into account in the context of suitability, aptitude and professional performance if they are useful for the intended activity. Applicants with severe disabilities will be given special consideration if they are equally suitable within the framework of the relevant provisions. We guarantee that your application documents will be destroyed in accordance with data protection regulations within six months of the end of the process. The collection and processing of personal data for the purpose of carrying out the application procedure is carried out on the basis of u00a7 23 of the German Data Protection Act. Hessian Data Protection and Freedom of Information Act (GDSIG) and Article 13 of Regulation (EU) 2016/649 of the European Parliament and of the Council of May 25, 2018 (General Data Protection Regulation). Supplementary information: Requirements for the applicant: Expert knowledge: Network administration, management, organization

VTS Orders & SAP Administrator (m/f/x) For our client, a world market leader in the metal and electrical industry, we are looking for a VTS Orders & SAP Administrator (m/f/x) for the Aalen location in full-time 35h as soon as possible. Your tasks: In addition to your work in Order Management, you will take on sub-project tasks for the successful implementation of SAP S/4 HANA with the following main activities: Order creation and processing incl. checking, e.g. release, delivery and invoicing Complaints processing / repair processing on the supplier side Carrying out inventories Sub-project tasks in the implementation of SAP S/4 HANA with the following tasks, among others: Defining requirements, identifying problems and developing target processes Support in the preparation of change management and the implementation of SAP S/4 HANA The requirements: A completed commercial apprenticeship or degree At least 3 years of relevant professional experience in supply chain / order management Excellent communication skills in German and English (other languages an advantage) Strong analytical skills Professional experience in logistics process analysis and optimization desirable SAP knowledge, ideally initial experience with SAP S/4 HANA Experience with process improvement and project management an advantage We offer: Above-tariff remuneration according to the IGZ tariff Fast and uncomplicated entry into a leading global company Very good chances of being taken on by the customer Possibility of a permanent employment contract Are you interested or have questions about the position? Please contact us by phone or e-mail at: 07961-968400 or [email protected] We look forward to receiving your application! Additional information: Requirements for the applicant: Basic knowledge: Project management, inventory, order acceptance, order processing, complaint processing Advanced knowledge: Supply chain management, SAP S/4HANA

ERP System Administrator (m/f/d) Project Manager (m/f/d) ERP The position is to be filled within the framework of temporary employment with the option of being taken on by our client You are also welcome to contact us by phone (05121 8090970) or WhatsApp (0152 36153951)! Your advantages with us: Permanent employment contract Remuneration from 19.00 EUR gross/hour depending on experience and qualifications Up to 30 vacation days per year depending on length of service Vacation and Christmas bonus Personal guidance and support at eye level, also by phone or WhatsApp (multilingual) Initial telephone consultation to assess your needs Non-binding job consultation Information about current job offers in your region Getting to know the potential workplace and client company High chances of being taken on by our client Job ticket What you can expect: Project management for the introduction and integration of production processes Contact person for 3rd level support Collaboration in the introduction of an MES and PDA system Implementation of 1st and 2nd level support What you should bring with you: Completed studies in the IT field or a comparable qualification Good understanding of operational processes Comprehensive knowledge of common ERP systems Leadership competence Company text The akut... Kompetente Lösungen GmbH was founded in 2000 and since then has been offering customized concepts with personal and partnership-based employee and customer support. As an owner-managed service provider, we stand for continuity and long-term orientation. We offer you contacts to interesting companies and accompany you on your next career step. We concentrate on your needs and thus achieve the best quality of placement. Your wishes are the focus of our collaboration!

Are you not only looking for a new professional position, but are you striving to take your passion for technology and administration to the next level? Then this position is just right for you! We are looking for an IT System Administrator Professional (m/f/d) for our prestigious client company in the housing industry in Wiesbaden. Exciting projects, innovative technologies and an inspiring working environment await you here. Become part of our team, master technical challenges with creativity, actively shape the future of system administration and develop your full potential! Take advantage of this unique opportunity and apply today! This position is to be filled as part of a direct placement / recruitment agency. IT System Administrator (m/f/d) in real estate development - hybrid working (remote & presence) Your tasks: You will be responsible for the administration, maintenance and documentation of the company's physical and virtual infrastructure in the areas of network, server, clients and software You further develop the company's IT environment You provide services for the specialist departments, participate in projects and sometimes also take over project management You take care of the provision of application systems and standard services You carry out the patch management of software components and manage all assets including the procurement process You supervise and support the 2nd/3rd level employees Your qualifications: You have a degree in (business) informatics or comparable training in an information technology profession with several years of experience in IT You have good to very good knowledge of MS Windows (client/server), MS Exchange, Microsoft SQL Server, VMWare (virtualization), Citrix, Netapp storage, software distribution (maintenance, deployment, patching), backup (Veeam, Veritas Backup Exec), network & client security (firewall, VPN) and VOIP telephony Swyx (Enreach) On Premise You have project experience You are characterized by your high social, consulting and communication skills You are a team player and able to work under pressure You have a strong service attitude You benefit from a high work-life balance through the collective agreement You work in a flexible annual working time model and with flexitime You will experience a human, open and constructive working atmosphere with flat hierarchies You take part in the internal training program and external training measures You have access to health management You will experience a pleasant working atmosphere and an appreciative corporate culture You will receive a free job ticket You have access to a vehicle pool for appointments on site After your individual training, you will have the opportunity to work remotely You will take on interesting, varied and responsible tasks With us, your career path will become your personal walk of fame - we offer you exciting prospects in the areas of assistance & secretarial services, marketing, sales, HR and purchasing & logistics. Click on \"Apply directly\" now!

System Administrator Linux and Windows (m/f/d) Allgeier Public is one of the leading full-service providers for digitization projects for public administrations in Germany. Our teams with around 500 colleagues shape the digital transformation of public administration and support our customers with expertise, advice and solutions. Join Allgeier Public and develop the future with us Germany with us! Become part of our team and start at Allgeier Public immediately at Munich location as System Administrator Linux and Windows (m/f/d). Your tasks Configuration and administration of Linux and Windows servers Administration of network components, switches and firewalls Supporting the team in the test lab Coordination with the customer in the area of process optimization and requirements Creation of the documentation Your profile Completed studies or completed vocational training with several years of professional experience in the IT environment Several years of practical experience in the administration of Linux and Windows systems Completed certification in Microsoft or Cisco is an advantage Good written and spoken German language skills Your advantages Mobile working: Depending on the project, mobile working is possible with us by arrangement. Family-friendly: We top up your salary to 100% if your child is ill. There is also the option to arrange an individual childcare allowance. Vacation days: 30 vacation days are a matter of course for us. Job ticket: So that you can easily reach our locations, we also support you with a subsidy for the Deutschlandticket. Culture: We live the \"Duz\" culture, have short communication channels and are happy to help you with questions across departments. Employees refer employees: Do you know someone in your circle of friends or family who is looking for a job? Your recommendation will definitely be rewarded. Even more benefits: possibility of a company pension scheme within our attractive group contract with an employer contribution of 20%, employee discounts, gifts for personal occasions. For further information on this and other offers, please contact us at any time. In order to guarantee quick processing, please quote reference number 149854.

Assistant to Head of Spare Parts / Project Administrator (m/f/d) Job code The KMS Group is a service company in the field of Human Resources. Our portfolio includes temporary staffing, recruitment, outsourcing and onboarding. site management in the fields of aviation, vehicle construction, mechanical engineering, steel construction, warehousing/logistics, finance/office and engineering. We offer you an innovative and challenging workplace, an attractive salary and good development opportunities. We are looking for you as an enthusiastic and reliable employee (m/f/d) for one of our customers in the field of: Mechanical Engineering at the Augsburg site, for a committed and motivated personality to join the team at the earliest possible date. Your tasks Supporting the Head of Spare Parts in all organizational and administrative matters Organization of meetings, workshops and business trips (including travel expense accounting) Creation of evaluations, status reports and professional presentations Creation and monitoring of customer contracts Independent implementation of projects Collaboration on special projects for the specialist area Your qualifications Completed commercial or business management training Several years of professional experience in the assistance and project area Experienced handling of MS Office Solution-oriented and independent way of working Good written and spoken English skills High level of reliability and trustworthiness Strong communication and teamwork skills, high level of discretion We offer An exciting challenge in a dynamic, internationally successful company a permanent position with us and, if you perform very well, the chance of being taken on by our client Very good pay in line with performance Up to 30 days vacation depending on length of service Company pension scheme Development and training opportunities on/off the job HAVE WE PIQUED YOUR INTEREST? Then we should definitely get to know each other! Start a career for your future with us. Apply now( https://kmszeitarbeit3.hr4you.org/job/apply/9372?page_langde ) KMS Zeitarbeit GmbH Niklas Baltrusch Niklas Baltrusch Augsburg branch Zimmererstrasse 20 86153 Augsburg 0821 45 44 37 - 18 [email protected]

Die Calderys Gruppe ist ein weltweit führender Anbieter für Industrien, die unter Hochtemperaturu00adbedinu00adgunu00adgen arbeiten. Calderys ist auf den Wärmeschutz von Industrieanlagen spezialisiert und bietet eine breite Palette an feuerfesten Produkten und fortschrittlichen Lösungen zur Verbesserung von Stahlguss, metallurgischen Flussmitteln und Formgebungsu00adverfahren. Als internationales Unteru00adnehmen bieten wir unseren mehr als 6.500 Mitarbeitern an unseren verschiedenen Standorten auf über 5 Kontinenten eine Welt voller Möglichkeiten.Wir setzen unser über 150-jähriges Know-how ein, um eine positiveu00adu00adu00ad Wirkung für unsere Stakeholder zu erzielen. Jeden Tag arbeiten wir an einer nachhaltigen Zukunft durch Teamarbeit, Kundenu00adorientierung und eine proaktive Denkweise. Wir sind ein Unternehmen, in dem Leistung anerkannt und Lernen gefördert wird; ein Umfeld, in dem Sie wachsen und Ihr Potential entfalten können. Ein Arbeitsplatz, an dem jeder Tag ein neuer Tag ist und an dem es niemals langweilig wird. Project Service Administrator - Projektsachbearbeiter (m/w/d) Neuwied, Rheinland-Pfalz, Germany Mission:Für unser Projektteam in Neuwied suchen wir Sie als Project Service Administrator, um unsere Montageprojekte abzuwickeln. In dieser Rolle sind Sie u.a. für die Erstellung von Angeboten in SAP, die Bearbeitung von Kundenbestellungen mit dem Projektleiter sowie die Versandabwicklung zuständig. Verantwortlichkeiten:Erstellen von Angeboten in SAPBearbeitung von Kundenbestellungen in Zusammenarbeit mit der Projektleitung (Einholen von Lieferantenerklärungen, Montagebestellung von Subunternehmen, Versandabwicklung etc.)Unterstützung des Controllings beim Monats- und JahresabschlussUnterstützung der Projektleiter bei der Abwicklung von Montageprojekten (Dokumentation, Zuarbeit in der Qualitätssicherung, Rechnungsstellung, Koordination verschiedener Schnittstellen etc.) AnforderungenAbgeschlossene kaufmännische AusbildungMin. 3 Jahre Erfahrung in der administrativen Abwicklung von ProjektenErfahrung mit Google Workspace, MS Office 365, SAP (R3)Gute Deutsch- und Englischkenntnisse notwendigGute Kommunikationsfähigkeiten Ihre VorteileArbeitgeberfinanzierte betriebliche AltersvorsorgeVermögenswirksame LeistungenGruppenunfallversicherungHybrides Arbeiten30 Tage UrlaubGute Erreichbarkeit und kostenlose ParkplätzeCorporate Benefits Ihr KontaktJETZT ONLINE BEWERBENWeitere Informationen darüber, was uns ausmacht, finden Sie auf calderys.com.

IT-Project Manager (all genders) Schwerpunkt CRM Vollzeit | Services | Augsburg Über unsDie baramundi software GmbH ist ein dynamischer Spezialist für IT- und OT-Lösungen. Seit Gründung im Jahr 2000 entwickeln und vertreiben wir innovative Endpoint-Management-Software und -Services Made in Germany. Kernprodukt ist die u201ebaramundi Management Suiteu201c. Aktuell verwalten Administrator:innen in mittelständischen Unternehmen und Organisationen weltweit damit ca. 3 Millionen Endpoints sicher und effizient. Über 290 Mitarbeitende in Deutschland, Großbritannien, u00d6sterreich, Schweiz, Polen, Italien und den USA engagieren sich dafür, die baramundi Management Suite mit Leidenschaft zu entwickeln, zu vertreiben und unsere Kunden mit umfangreichem Service zu unterstützen. Wir freuen uns, dich kennenzulernen! Willkommen bei baramundi! u201eGib unseren Projekten deine Handschrift.u201cEine der wichtigsten Konstanten bei baramundi? Abwechslung. Ob Sales, Marketing, Finance, Support, Services oder Entwicklung: Unsere Abteilungen sind dein Fachbereich. Genau wie das Entwickeln, Managen und Optimieren von Projekten. Deine Expertise macht Abläufe rund und Projekte erfolgreich. Der dynamische baramundi Spirit in unserem PMO & BA Team hilft dir dabei. So wird aus Daily Work Teamwork. Und daraus der perfekte Workflow. Tu, was du am besten kannst:PLANEN Du verantwortest die Planung und Steuerung unterschiedlichster interner IT-Projekte und stellst den Projekterfolg unter Einhaltung der vereinbarten Termin-, Budget- und Qualitäts-Zielen sicherINNOVATIV DENKEN Du bist maßgeblich daran beteiligt, unsere Business Applikationen Schwerpunkt CRM und Sales-Prozesse innovativ weiterzuentwickeln und zu digitalisierenETWAS BEWEGEN Du unterstützt aktiv die Projektumsetzung und treibst diese voranBERATEN & BEGLEITEN Enge Beratung und Abstimmung mit den beteiligten Fachbereichen sowie das Management von externen Dienstleistern und Softwarelieferanten AUSTAUSCH PFLEGEN Du kommunizierst und koordinierst zwischen allen Stakeholdern und präsentierst Projektergebnisse souverän auf Management EbeneVORAUSSCHAUEN Die Mitwirkung bei der Projektportfolio- und Budgetplanung sowie bei der Weiterentwicklung von internen Projektmanagement- Methoden und -Standards runden Deine Aufgaben abSPASS HABEN Du findest deinen Platz in unserem bunten und kollegialen Umfeld Bring mit, was wir an dir schätzen:Abgeschlossenes Studium der Informatik, (Wirtschafts-)Informatik oder BWL, alternativ eine vergleichbare Ausbildung mit Berufspraxis Mehrjährige Berufserfahrung in der Leitung von Projekten sowie sicherer Umgang mit klassischen und agilen ProjektmethodenGrundlegende Kenntnisse von ERP- und CRM-Systemen Unternehmerisches Denken und Handeln sowie informationstechnisches VerständnisSpaß an komplexen Themen und eine ausgeprägte Hands-On und ServiceorientierungKommunikations-, Präsentations- und ModerationskompetenzSehr gute Deutsch- und Englischkenntnisse runden dein Profil ab So ticken wir! 10 Gründe für deinen Einstieg bei baramundi!#1 KOMM' IN RUHE AN Unser Rundum-Sorglos-Paket macht den Einstieg besonders leicht. Deine persönliche:r Startbegleiter:in zeigt dir alles: vom Welcome-Frühstück bis zum vollausgestatteten Arbeitsplatz. #2 FÜHL DICH ZUHAUSE Das Mittagessen im hauseigenen Restaurant baraGusto und viele leckere Kaffeevariationen im gemütlichen Cafu00e9Mundi gibt es kostenlos. Wir kümmern uns um deine Post und Pakete. Einmal im Monat treffen sich alle baramundianer während der Arbeitszeit zum Pizzaessen und Quatschen. Einfach so. #3 ERFAHRE WERT UND WERTSCHu00c4TZUNG Wir glauben an Werte und leben sie: Miteinander und Vertrauen. Mut, Begeisterung und Kompetenz. Unsere Kommunikations-Kultur ist offen und ehrlich. Genau wie die regelmäßigen Team-Feedbacks. #4 LASS DICH BELOHNEN Unsere Anerkennung spürst du auch. Erfolgs-Boni ist ebenso selbstverständlich wie Weihnachtsgeld, betriebliche Altersvorsorge und Teamevents. #5 GENIESSE DAS LEBEN Arbeitszeit ist Lebenszeit. Deshalb darfst du sie bei uns individuell gestalten. Mit Gleitzeit in Voll- oder Teilzeit, Home-Office, Mobile Work und sogar Sabbatical-Option. Bei einer 37 Stunden Wochenarbeitszeit mit 30 Tagen Urlaub. #6 BLEIB GESUND Wir wollen, dass es dir gut geht. Deshalb haben wir ergonomische Möbel und organisieren Gesundheitstage, Massagen, Yoga- und Laufgruppen. #7 ENTWICKLE DICH WEITER Dein persönliches und fachliches Weiterkommen ist uns wichtig. Wir bezahlen Fortbildungen, Sprachkurse und Coachings während der Arbeitszeit. Sogar 2-jährige Arbeitsaufenthalte in unserer Niederlassung in den USA sind drin. #8 ARBEITE AUF AUGENHu00d6HE Wir sind alle per du, vom Azubi bis zur Geschäftsführung. Komplizierte Hierarchien gibt es bei uns nicht. #9 DEINE FAMILIE IST UNS WICHTIG Familie bedeutet bei uns da sein, sich kümmern und gegenseitig unterstützen. Das tun wir mit Kita-Zuschüssen und Ferienbetreuung genauso wie bei unserem Familien-Sommerfest. #10 MACH UNS NOCH BESSER Wir wollen ein großartiger Ort und Arbeitgeber sein. Dazu brauchen wir ehrliches Feedback. Du hast Anregungen und Ideen, die uns noch besser und glücklicher machen? Wir setzen sie um. Kontaktiere uns! Kontaktiere uns!Deine persönliches Recruiting-Team Giulia Di Chiazza, Alexandra Wagner, Doris Hoefflinger +49 821 5 67 08 - 150 Jetzt bewerben Jetzt bewerben

Public job advertisement The Office for Data Processing, Department of Statistics and Elections is seeking to fill the following position at the earliest possible date to fill the following position: Open data clerk (m/f/d) for statistics and R programming **** Requirement profile: 1. required is: a university degree (Diplom (FH) or Bachelor) in the field of data science, data analytics, business informatics, statistics or psychology or in another suitable subject area 2. desirable are: extensive knowledge of data analysis, statistical methods and statistical programming with R and R-Studio as well as RShiny/RMarkdown Applicable knowledge of database management systems (e.g. PostgreSQL), SQL programming and in the field of statistics and electoral law good cooperation with superiors and colleagues and the associated team-oriented behavior, very good comprehension and agility of thought, high resilience, good technical knowledge and skills in the area of responsibility as well as good quality and usability of the work results [The required certificates/certificates must be attached to the application documents as copies. If the required certificates are not enclosed, this will result in exclusion from the application process. Internal applicants are also requested to enclose the required evidence with their application documents]. **** The area of responsibility includes in particular 1. task-related instruction and coordination tasks in accordance with the distribution of responsibilities in particular Coordination of statistical data projects and clarification of fundamental technical issues in the area of responsibility Representation of the Statistics and Elections Department in working and project groups (e.g. supra-local joint projects for data connection and R programming (KO.R in the KOSIS network)) 2. conceptual design of the information offer and securing the provision of data, in particular Conception and expansion of the statistical information offered by the Erfurt city administration Coordination, planning and implementation of projects for the development of data from specialist procedures and external sources Determining and defining relevant data collection characteristics/data features for data development projects to carry out data analyses and compile statistics Development and updating of a concept (data strategy) for the further development of data skills (urban statistical literacy) **** 3. implementation of complex and R-programming based data analyses as well as development of a statistical R-programming based open data offer, in particular Carrying out complex data analyses using statistical methods Development and design of a statistical R-programming based open data portal Development of evaluation scripts and programming of graphic/dashboard applications using R and RStudio as well as R-Shiny/R-Markdown 4. implementation of difficult automation and evaluation routines using R programming, in particular Development of evaluation scripts using statistical methods Programming of automation routines Development of evaluation routines for empirical surveys and for register data Design of the election results presentation and automation processes using RStudio and RShiny/RMarkdown Coordination of election result collection and processing of election results 5. performing subtasks in the enforcement of data protection requirements, in particular Checking the accessibility of statistical information in compliance with statistical confidentiality Ensuring data protection compliance of the data to be accessed and collected Documentation of processing activities relevant to data protection In addition to an interesting and challenging job, we offer you Intensive support during your induction A flexible working time model 30 days of vacation per calendar year with a calendar week of five working days A company pension scheme in the supplementary pension fund Capital-forming benefits the possibility of educational leave in accordance with the Thuringian Educational Leave Act Further education and training opportunities Health-promoting and health-preserving measures as part of our company-wide training program health management **** Evaluation: E 11 TVöD (collective agreement for the public service)**** Application deadline: June 14, 2024 **** Apply online now via the homepage of the state capital Erfurt! ( http://www.erfurt.de/ef147739 ) **** Notes: Severely disabled applicants will be given preferential consideration if equally qualified. The Erfurt city administration wants to make a contribution to the advancement of women and therefore expressly encourages women to apply. If you are unable to apply online, please send your application documents to the Erfurt City Administration, Personnel and Organization Office, Meister-Eckehart-Strau00dfe 2, 99084 Erfurt. However, applications should primarily be submitted via the online service. Once the recruitment process has been completed, the applications of unsuccessful applicants will be duly deleted/destroyed in accordance with Section 27 (4) Thu00fcrDSG. Please also note the information on the collection of personal data, which can be viewed on the website \"Human Resources: Collection of personal data - Article 13 GDPR\" ( www.erfurt.de/ef139794 ). Supplementary information: Requirements for the applicant: Basic knowledge: PL/SQL programming language Advanced knowledge: Statistics, data analysis

Administrator:in IT Infrastructure Network m/f/d Contilia, based in Essen, is a non-profit group of companies in the healthcare sector that focuses on the areas of hospitals, senior living and care facilities, youth facilities, healthcare services as well as education and training. Contilia.Digital provides all IT services for the Contilia Group and its facilities. Strategically and operationally, we design the application and infrastructure landscape centrally in the project, operation and service stages for the approximately 7,500 users. We use enterprise components, solutions and services from renowned manufacturers and suppliers. Our experts implement interoperable processes and architectures with a focus on performance, stability and security. For the Infrastructure Operations team, we are looking for a:n dedicated:n Administrator:in IT Infrastructure (m/f/d) network Tender number: 10213 Your tasks Administration, operation, maintenance and performance tuning of the IT network infrastructure: LAN / WAN / W-LAN Switching and routing (e.g. 802.1X, BGP, OSPF, RPVST) Network segmentation / firewall VPN Ensuring service stability and service availability Development of new concepts, as well as analysis, further development and expansion of the existing network infrastructure Diagnosis and problem solving in the network elements as well as 2nd level support Joint implementation of IT infrastructure projects with internal and external teams, including taking on project management tasks Coordination and management of manufacturers and service partners in the event of faults / troubleshooting (3rd level) and installations Creation of project, system and application documentation Participation in the continuous improvement of service performance and quality Completed training in the field of IT Several years of professional experience in network administration, proven knowledge in the field of network protocols and techniques as well as conception of network architectures Sound know-how in the areas of routing and switching, as well as in the administration of firewall systems Good knowledge of controller-based W-LAN, NAC (802.1x), VPN and SDN Good comprehension skills and the ability to analyze complex contexts independently Communication skills and an open and courteous manner characterize you You have a structured and independent way of working and take a solution-oriented approach to problems The ability to work in a team and a strong service orientation round off your profile An attractive salary in accordance with AVR-Caritas including an annual special allowance A company pension financed by the employer at 5.6% of gross salary with the Kirchliche Zusatzversorgungskasse Köln (KZVK) Option of a discounted company ticket with Ruhrbahn Welcome event for our new employees Wide range of employee benefits and discounts (e.g. corporate benefits) Flexible participation in mandatory training courses through our e-learning program Numerous offers in our internal health management program Regular training and further education Curious? If you have any questions, please call Lars Jakubowski, Head of Infrastructure, Operations & Services, on +49 201 65056-4532. We look forward to hearing from you!

Administrator:in IT Infrastruktur Clientmanagement m/w/d Die Contilia mit Sitz in Essen ist eine gemeinnu00fctzige Unternehmensgruppe im Gesundheitswesen, die sich auf die Bereiche Krankenhu00e4user, Seniorenwohn- und Pflegeeinrichtungen, Jugendeinrichtungen, Gesundheitsservices sowie die Aus- und Fortbildung konzentriert. Contilia.Digital erbringt alle IT-Dienstleistungen fu00fcr die Contilia Gruppe und ihre Einrichtungen. Strategisch und operativ gestalten wir die Applikations- und Infrastruktur-Landschaft zentral in den Stadien Projekt, Betrieb und Service fu00fcr die ca. 7.500 Anwender:innen. Hierzu setzen wir Enterprise-Komponenten, -Lösungen und Dienstleistungen namhafter Hersteller und Lieferanten ein. Unsere Expert:innen realisieren interoperable Prozesse und Architekturen mit Schwerpunkt auf Performance, Stabilitu00e4t und Sicherheit. Fu00fcr das Team Infrastruktur-Betrieb suchen wir zum nu00e4chstmöglichen Termin eine:n engagierte:n Administrator:in IT Infrastruktur (m/w/d) Clientmanagement Ausschreibungsnummer: 10552 Ihre Aufgaben Administration, Installation, Betrieb, Wartung und Performancetuning von Clientsystemen Fat Clients Thin Clients Mobile Geru00e4te Softwareverteilung (M42) Endpoint Security Sicherstellung der Servicestabilitu00e4t und Serviceverfu00fcgbarkeit Entwicklung von neuen Konzepten, sowie Analyse, Weiterentwicklung der bestehenden Infrastruktur Diagnose und Problembehebung an den verschiedenen Clients Gemeinsame Umsetzung von IT-Infrastrukturprojekten mit internen und externen Teams Koordination von Herstellern und Servicepartnern bei Störungen / Fehlerbehebungen (3rd Level) Erstellung von System- und Anwendungsdokumentationen Mitwirkung bei der kontinuierlichen Verbesserung der Service-Leistungen und -Qualitu00e4t Abgeschlossene Ausbildung im Bereich IT Mehrju00e4hrige Berufserfahrung und nachgewiesene Kenntnisse in der System-Administration Gute Kenntnisse im Bereich Microsoft Windows, Igel-OS, Softwareverteilung, MDM und Endpoint Protection Gute Auffassungsgabe und die Fu00e4higkeit, komplexe Zusammenhu00e4nge selbststu00e4ndig zu analysieren Kommunikationsfu00e4higkeiten sowie eine offene und zuvorkommende Art zeichnen Sie aus Sie verfu00fcgen u00fcber eine strukturierte und eigenstu00e4ndige Arbeitsweise und gehen lösungsorientiert an Problemstellungen heran Teamfu00e4higkeit sowie eine ausgepru00e4gte Dienstleistungs- und Serviceorientierung runden Ihr Profil ab Spannende Projekte Die Möglichkeit sich einzubringen Eine attraktive Vergu00fctung gemu00e4u00df AVR-Caritas inklusive ju00e4hrlicher Sonderzuwendung Eine vom Arbeitgeber mit 5,6 % vom Bruttogehalt finanzierte Betriebsrente bei der Kirchlichen Zusatzversorgungskasse Köln (KZVK) Option auf ein vergu00fcnstigtes Firmenticket bei der Ruhrbahn Willkommensveranstaltung fu00fcr unsere neuen Mitarbeiter Vielseitige Mitarbeitervorteile und Rabatte (z. B. Corporate Benefits) Flexible Teilnahme an Pflichtschulungen durch unser E-Learning-Programm Zahlreiche Angebote in unserem betriebsinternen Gesundheitsmanagement Regelmu00e4u00dfige Fort- und Weiterbildungen Neugierig? Bei Ru00fcckfragen steht Ihnen Lars Jakubowski, Head of Infrastructure, Operations & Services, gerne telefonisch unter +49 201 65056-4532 zur Verfu00fcgung. Wir freuen uns auf Sie!

Join us and write your success story with us! For over 25 years, meco has been offering its customers IT solutions from a single source - from strategy consulting to day-to-day business management. With a wealth of experience, expertise and great passion, we work internationally for customers from various industries. They rely on us because we take a holistic, strategic approach and act pragmatically. Our motto is: meco makes it easy! It's easy - become part of the meco team! At the earliest possible date, we are looking for you for our location in Weingarten as: IT System Administrator with focus on VMware & Veeam (m/f/d) Simply exciting Exciting and varied tasks await you: Handling business trips and training courses Design, implementation and further development of virtualization solutions based on VMware & Veeam System management of virtualized infrastructures Development and implementation of storage and backup concepts Implementation of customer projects in the VMware and Veeam environment Virtualization/ Cloud Storage, SAN network Backup Monitoring Server/client systems Consulting, planning and implementation Creation of project and concept documents Service/maintenance of systems Documentation Support Technical project management/project responsibility in coordination with the team leader Traveling, installations at the customer's site Simply join in To join our team, you need the following: Completed IT training, e.g. as an IT specialist in system integration Initial experience with VMware components desirable, we will develop everything else together Independent way of working as well as high service orientation and commitment Continuous further development is important to you Good German and English skills round off your profile You are characterized by commitment and reliability Simply feel good So that you feel comfortable with us, we offer you: A secure job in a collegial working environment Reliable and flexible working time model 30 days vacation + special leave Performance-related pay Responsible tasks in a family-run company in the region Variety, new challenges and responsibility Short communication channels thanks to a flat and familiar company structure Individual development and training opportunities Mobile working Capital-forming benefits & company pension scheme Free coffee and tea variations, as well as soft drinks and water dispenser Bicycle leasing, corporate benefits, loyalty bonuses, employee events Do you not have all of these skills or are you a career changer? No problem, let's talk! Simply apply Join us and send us your application. We look forward to getting to know you soon. meco IT GmbH Liebfrauenstrau00dfe 8 88250 Weingarten | Phone +49 751 79132 174 | [email protected]

System Administrator (m/f/d) Job introduction For a partner based in Hamburg, we are looking for an IT System Administrator (m/f/d) with knowledge of process management to start as soon as possible on a direct placement basis. You have a goal - we have the jobs mika stands for employee- and customer-oriented work. We open the doors of the most sought-after companies in various industries. Almost all employees are offered permanent employment. Depending on your personal qualifications and wishes, we will work with our customers to find the right position for you, and we stand for reliability, fairness, honesty and respectful treatment. Our client offers: Direct, permanent entry into an internationally active company in the logistics industry an attractive work location in the Kontorhaus district of HH and hybrid working An above-average remuneration package A starter bonus after the probationary period Your tasks: Project management IT area IT process planning and the implementation / realization of processes Software administration, maintenance, planning and configuration for the internal IT infrastructure Internal user support with ticket system (1st + 2nd level support) Support / further development of company applications Your qualifications: Training as an IT specialist/system administrator or practical knowledge Experience in project management Service orientation and resilience \"Hands-on mentality\" and proactive way of working Good knowledge of German and English Andreas Fuchs looks forward to receiving your application via our online portal or by email to: [email protected] . Do you need more information? We can also clarify your questions in advance by telephone.