Überblick über die Statistik des Gehaltsniveaus für "Project Coordinator 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

Curious about the future of event marketing?SpotMe is the enterprise event platform to manage engaging events that help accelerate customer relationships at scale. Trusted by 12,000+ global Fortune 500 business leaders and loved by 10,000,000+ users, brands like J&J, Deloitte, and Red Hat use SpotMe to manage hybrid, virtual, and in-person events with a branded, personalized and compliant experience and get deep data insights that flow into their CRM.Behind the magic stands a curious, diligent, and humble team with over 30 nationalities. A team that feels great pride in the work they do, a team that cares for each other, and a team that is always ready for the next challenge.Mission:Support in delivering Onsite, Virtual, and Hybrid eventsResponsibilities:Onsite supportRequired frequent travel to destinations worldwide.Provide assistance to participants.Set up and deliver live interactivity.Set up and rehearse onsite with the client and AV team before the event.Facilitate engagement activities.Act as the primary point of contact with the client onsite.Update content to the app whilst onsite.Virtual support Schedule and deliver speaker briefing sessions.Participate/Lead the project kick-off and reviews with the project lead and clients.Run speaker green rooms during live sessions.Use our powerful Backstage CMS to tailor-make the clients’ apps and to ensure the best participants' experience before, during, and after the event.Be the main point of contact for the client during live sessions, handling platform updates and user escalations.Live monitoring of the platform and reporting on the metrics of the event.Fully manage and deliver small-scale projects.This role can potentially lead up to a Project Manager position (still contractor based).Requirements:At least two years experience in event management (stage management, speaker coordination, other relevant).Demonstrable experience of onsite event management or coordination.Have a modern computer, equipped with Google Chrome and MS Office.If using a Mac, Apple M1 Processor and 16 GB RAMIf using a PC, Intel i7 processor and 16 GB RAM.Have a stable Internet connection (wifi / wired), with a bandwidth of at least 20Mbps down, 10Mbps up.A mobile with 4G / 5G to fallback on if needed.Eligible to travel internationally.Clean basic background check.At least 18 years old.Based in Germany.Accessible to a major international airport.Fluent in English. Fluent also in German.Registered as a sole trader, self-employed, or owner and employee of your company, in Germany.More information:You can find more information here:Technical assessment and supporting resources detailsOur Talent Network FAQSpotMe recruits, compensates, and promotes regardless of race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, parental status, or veteran status.

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

Deine AufgabenDu bist verantwortlich für die Projektplanung und Task-ErstellungDu übernimmst die tägliche Anpassung & Pflege unseres PlanungstoolsDu bist zuständig für unsere Zeit- und Ressourcenplanung inkl. QualitätsmanagementDu bist der Sparringspartner für unsere Account Manager, Design und Content DirektorenDu kümmerst dich um unsere internen ProjekteDein ProfilDu hast ein abgeschlossenes Studium oder eine erfolgreich abgeschlossene Ausbildung Du hast bereits Agenturerfahrung im digitalen UmfeldDu hast erste Erfahrung in der Betreuung von KundenprojektenDu kennst Dich aus im digitalen MarketingDu beherrschst gängige Planungstechniken und ToolsOrganisieren liegt Dir im Blut Du hast deine Stärken und Spaß an strukturiertem, selbständigem und eigenverantwortlichem ArbeitenStrukturiertes, selbstständiges und eigenverantwortliches Arbeiten zählt zu Deinen Stärken und bereitet Dir FreudeDu denkst konzeptionell und hast ein technisches GrundverständnisDu hast ein gesteigertes Qualitätsbewusstsein und bist den Entwicklungen im digitalen Marketing gegenüber aufgeschlossenMit Deinem Auftreten kannst Du andere begeistern und bist kommunikationsstarkDu hast sehr gute Deutschkenntnisse in Wort und Schrift und Deine Englischkenntnisse enden nicht bei "Hello“ und "Goodbye“Wir trauen Dir Großes zu! Bei uns kannst Du vieles lernen. Daher freuen wir uns auch dann über Deine Bewerbung, wenn Du nicht alle Punkte erfüllst.Das kannst Du von uns erwartenEin dynamisches und spannendes Agenturumfeld mit wirklich tollen Kollegen und einer fairen Work-Life-Balance. Denn wir wollen, dass Du lange bei uns bleibst!Kontinuierliche Aus- und Weiterbildung im sich am schnellsten entwickelnden Umfeld der digitalen MedienlandschaftFlache Hierarchien und schnelle Übernahme von VerantwortungHervorragende AufstiegsmöglichkeitenModerne und hochwertige ArbeitsausstattungWir bieten Dir flexible ArbeitszeitenDu hast die Wahl! Home-Office oder OfficeBenefitsDynamisch, aktiv und immer einen Schritt voraus: Damit es allen unseren fleißigen und motivierten Köpfen rundum gut geht, sorgen wir für abwechslungsreiche Aktionen und attraktive Annehmlichkeiten.Urban Sports Mitgliedschaft mit ArbeitgeberzuschussNextbike Mitgliedschaft mit 60 Freiminuten pro AusleiheCorporate Benefits Mitarbeiterrabatte für diverse Online ShopsNimm Dir Zeit für Dich: 2 Mental Health Days pro Jahr & regelmäßig mobile Massage im OfficeUnbegrenzter Zugang zu Trainings auf LinkedIn Learning Familienservice von voiio: Plattform mit Angeboten wie virtueller Kinderbetreuung, Yoga Sessions und vielfältigen BeratungsangebotenMitarbeiter-Café mit leckerem Kaffee, Getränken, einer Müsli-Bar und frischem ObstTolle Parties, Agentur-Events und Kicker-Turniere Über unsAls unabhängige Marketing-Agentur steht add2 für digitale Kommunikation. Von A bis Z. Seit 1997 lotsen wir unsere Kunden durch digitale Gewässer wie Content- und Social-Media-Marketing, Dynamic Video und Audio oder Display- und Programmatic-Advertising. Was immer unsere Kunden bewegt, gemeinsam sorgen wir für die passende Lösung. Hand in Hand und immer mit dem Blick aufs Ganze. Unsere bunt gemischte HafenCrew besteht aus Menschen mit den unterschiedlichsten Talenten. Du kannst also auf jede Menge Know-how aus vielen Köpfen zurückgreifen. So lernen wir täglich voneinander und arbeiten dabei eng zusammen. Wie du siehst, wird der Teamgedanke bei uns großgeschrieben. Den möchten wir durch gemeinsame Aktivitäten wie Agentur-Events, Team-Essen und Feierabendbiere in gemütlicher Runde fördern. Und das Beste: Wir arbeiten da, wo andere Urlaub machen. Mit direktem Blick auf den Medienhafen können wir auch mal abschalten und kreative Gedanken tanken. Und wenn das nicht ausreicht, bietet dir unser gemütliches Mitarbeitercafé mit Kicker, kostenlosem Obstkorb und Getränken das perfekte Ambiente, um sich mit deinen Team-Kollegen und Kolleginnen auszutauschen. Solltest du einmal im Home-Office sein, dann kannst du dich einfach über Teams mit deiner Hafen-Crew austauschen. Standort add2 GmbH, Düsseldorf

Lyric Automation Germany GmbH, with its locations in Hamburg, Langenhagen near Hanover, and Munich, specializes in sales, project management and after-sales service for high-quality automation systems and acts as a link between the parent company Guangdong Lyric Robot Automation and the European market. Lyric Robot is a high-tech company with over 10,000 employees and is a manufacturer of high-end automation systems in the areas of automotive and consumer batteries, automotive parts, precision electronics and rail transport. The company has a dominant position in the Chinese market and also exports its intelligent manufacturing solutions to Europe, the USA, Canada, Mexico, Japan, India and the Middle East.AufgabenBills and Contracts management.Financial records and reports preparationFinancial software management, for example, DATEV, SAPResponsible for sorting out VAT issues and communicating with tax accountants on various financial issues.Responsible for preparing project technical service contracts and pre-sales service contracts.Budget and cost management.Bank and financing communication, handling related consultations such as guarantee financing.Assisting our HQ to transfer funds to overseas and other subsidiaries and affiliated companies legally and compliantly.Audit work cooperation.QualifikationFinancial expertise: In-depth understanding of German accounting and tax regulations as well as basic knowledge of international financial standards. Analytical and problem-solving skills: Ability to analyze financial data, identify potential problems and develop effective solutions.Communication skills: Fluent in English and German, knowledge of Chinese is an advantage. Clear, accurate and effective communication with internal team members, external partners (such as banks, tax advisors) and international colleagues (China, Poland) is required.Knowledge of financial software and office software: Basic knowledge of the financial software DATEV and skilled use of office software such as Excel to process complex tables and financial reports.Teamwork: Working with team members to complete projects and tasks together. Intercultural communication skills: The ability to communicate effectively and work in different cultural contexts is very important due to international coordination.If you enjoy designing or independently developing your area of responsibility, we would like to get to know you. Please send us your documents, your salary expectations, and your possible starting date.Your contact for your application:Jiefei Shi, HR departmentLyric Automation Germany GmbHDie Lyric Automation Germany GmbH mit ihren Standorten in Hamburg, Langenhagen bei Hannover, und München ist auf den Vertrieb, das Projektmanagement und den After-Sales-Service von hochwertigen Automatisierungsanlagen spezialisiert und fungiert als Verbindung der Muttergesellschaft Guangdong Lyric Robot Automation zum europäischen Markt. Lyric Robot ist ein High-Tech-Unternehmen mit über 7.000 Mitarbeitern und ist Hersteller von High-End-Automatisierungsanlagen in den Bereichen Automotive- und Consumer-Batterien, Automobilteile, Präzisionselektronik und Schienenverkehr. Das Unternehmen verfügt über eine dominante Position im chinesischen Markt, exportiert seine intelligenten Fertigungslösungen auch nach Europa, die USA, Kanada, Mexiko, Japan, Indien und in den Mittleren Osten. Standort Lyric Automation Germany GmbH, Langenhagen

ZEIT MEDIA.ZEIT MEDIA ist die Sales Organisation der ZEIT Verlagsgruppe. Unsere Mission: Gemeinsam stark kommunizieren. Uns interessiert, was unsere Kund:innen bewegen möchten. Gemeinsam entwickeln wir kraftvolle Kommunikationslösungen, um die richtigen Zielgruppen optimal über alle Medien-Kanäle der ZEIT zu erreichen.Verbinde Marken und Inhalte.DIE ZEIT Verlagsgruppe wächst kontinuierlich und stellt dazu ihre Vermarktung noch zukunftsorientierter auf. Nutze diese Chance und werde Teil dieses erfolgreichen Teams! Zur Unterstützung unseres Teams in Hamburg suchen wir zum nächstmöglichen Zeitpunkt und in unbefristeter Anstellung einen Concept Coordinator (d/w/m) in Vollzeit.Als Concept Coordinator berichtest du an den Head Brand & Concept Solutions im Bereich ZEIT MEDIA und übernimmst schwerpunktmäßig die folgenden Aufgaben:Du bist als Projektmanager und One-face-to-the-customer​ verantwortlich für die professionelle Umsetzung portfolioübergreifender Mediakonzepte.Du unterstützt das Concepter-Team bei der Erstellung kreativer, kundenindividueller Mediakonzepte nach Briefing der Media Sales Manager bzw. anhand von Kunden- oder Mediaagentur-Briefings.Du setzt die Projekte nach Abschluss professionell um. Von der Vertragserstellung über Kampagnenoptimierung bis zum Reporting und die Koordination und Steuerung aller beteiligten Gewerke liegt die Verantwortung bei dir.Du hast den Überblick über alle Produkte, Marken, Ad Specials und weitere Angebote innerhalb des ZEIT MEDIA-Portfolios.Du kannst die Kundenbedürfnisse gut einschätzen, so dass du durch die Projektbetreuung Potentiale für Upselling und Anschlussprojekte erkennst und dem Sales Manager mitteilst.Crossmedial und kommunikationsstark - Dein Profil.Du verfügst über ein abgeschlossenes kommunikationswissenschaftliches oder medienwissenschaftliches Studium oder eine adäquate praxisorientierte Ausbildung.Idealerweise hast du bereits mehrjährige Berufserfahrung im B2B-Marketing eines Medienunternehmens oder einer Kommunikationsagentur gesammelt und bringst daher Erfahrung in der Nutzung von Projektmanagementtools mit.Du hast Erfahrung in der Koordination und Steuerung von Projektteams und begreifst die Betreuung komplexer Themen und anspruchsvoller Kunden als Chance.Durch deinen crossmedialen Hintergrund siehst du die digitale Transformation des Medienmarktes als Chance. Du trittst selbstbewusst auf und zeichnest dich durch deine Kommunikationsstärke und deine Offenheit für Neues aus. Du überzeugst uns mit einer schnellen Auffassungsgabe, einer strukturierten und gründlichen Arbeitsweise.Klingt nach dir? Dann freuen wir uns über deine Bewerbung inkl. einem aussagekräftigen CV sowie Arbeitszeugnissen.Unser Engagement für deine Entwicklung.Dazulernen: Weiterbildung ist uns wichtig. Deshalb bieten wir allen Mitarbeitenden über unsere ZEIT AKADEMIE, die Produkte von ZEIT SPRACHEN, dem Holtzbrinck E-Learning Campus oder Blinkist vielfältige Möglichkeiten zur individuellen Entwicklung. Einmal im Jahr nutzen wir den internen ZEIT University Day sowie regelmäßige University Snacks, um uns zu verschiedenen Themen auszutauschen und voneinander zu lernen.Arbeitsort und - zeit nach individuellen Bedürfnissen: Unsere Arbeitsumgebung ist geprägt von Flexibilität und Individualität. Wir bieten flexible Arbeitszeiten wie Gleitzeit und mobiles Arbeiten sowie vielfältige Teilzeitmodelle, um die Balance zwischen Beruf und Privatleben optimal zu gestalten. Zusätzlich befinden sich unsere Arbeitsplätze in zentraler Lage mit exzellenter Anbindung an den öffentlichen Nahverkehr – einen Zuschuss zum Deutschlandticket und für ein JobRad gibt es natürlich auch.Vergünstigungen: Wir lieben unsere Produkte, daher steht dir die gesamte Bandbreite unserer Publikationen, Veranstaltungen und Medienangebote kostenfrei zur Verfügung. Zusätzlich bieten wir zu Mitarbeiterkonditionen verschiedene Zeitungs- und Zeitschriftenabonnements sowie unsere ZEIT Shop Produkte an. Über die Plattformen Corporate Benefits und benefit.me kannst du außerdem von vielen Vergünstigungen für Museen, Theater, Festivals, verschiedene Produkte oder Konferenzen profitieren. Individuelle Unterstützung: Das ganzheitliche Unterstützungsprogramm “Employee Assistance Program“ bietet Dir schnelle und wirkungsvolle Hilfe bei beruflichen und privaten Fragestellungen – auch in besonderen Krisensituationen.Kommunikation und Austausch werden bei uns großgeschrieben. Durch verschiedene interne Formate und Projekte, wie z.B. unserem Mentor:innen - und Pat:innen-Programm, einem monatlichen All Hands und begleitenden Newslettern oder beim Mystery Lunch fördern wir Vernetzung und Austausch. Erste Einblicke findest du bei kununu, LinkedIn ,  XING oder auch auf unserer  ZEIT Karriereseite. Solange diese Position auf unserer Karriereseite sichtbar ist, kannst du dich sehr gerne darauf bewerben - es gibt keine Bewerbungsfrist. Weitere Antworten zu unserem Bewerbungsprozess findest du in unseren FAQ. Wir kümmern uns umeinander.Die ZEIT Verlagsgruppe ist ein Arbeitgeber, der für Chancengleichheit und einen respektvollen Umgang steht. Wir setzen uns ein für faire Beschäftigungsmöglichkeiten unabhängig von ethnischer oder sozialer Herkunft, Geschlecht, Religion, Weltanschauung, Alter, sexueller Identität oder Behinderung. Unser stetiges Ziel ist es, ein wertschätzendes und anerkennendes Arbeitsumfeld für alle Beschäftigten zu schaffen. Über das Unternehmen:Zeitverlag Gerd Bucerius GmbH & Co. KG

Abiomed is an innovative medical device business with an inspiring mission "Patients First" and a unique guiding company principle "Recovering hearts. Saving lives." With more than 2,000 employees, Abiomed is one of the fastest growing medical technology businesses in the world with corporate headquarters in Danvers, USA, and locations in Aachen and Berlin, Germany, Tokyo, Japan, and Singapore. Abiomed is part of Johnson & Johnson MedTech.Abiomed is an employer with attractive working conditions and an appreciative corporate culture that focuses on the needs of its employees. Abiomed inspires and retains exceptional talent through collaboration, passion and continuous development.Clinical Trial CoordinatorThe Clinical Trial Coordinator (CTC) supports Clinical Project and Program Managers in planning and coordinating activities in all aspects of clinical trial operations. This position requires appropriate interpretation of significant policies and procedures. It involves interaction with internal and external customers and partners, and must operate with a high degree of discretion, as the role involves handling information of a confidential and critical nature.Main tasks and responsibilities:Plan, coordinate, and arrange study communications and meetings on and off-site with both internal and external attendeesPrepare all necessary documents for the evaluation of new proposals and coordinate the decision process of new AR or ISS projectsManage the grant application platform which maintains all necessary documents and the communication with PIsSet up, update, maintain and close Trial Master Files. Assure currency and accuracy of required clinical trials documents Maintain project-specific regulatory document inventory systems which include a precise quality check (QC) process when documents are receivedCommunicate with investigator sites on collection of regulatory documentsCreate study materials, including newsletters, study updates, etc. under the direction of a Scientist or Clinical Program ManagerSource and distribute study suppliesInteract with Finance departments to support invoice processingInteract with the Sales and Customer service department to support and coordinate external needs and internal processes.Under guidance of Clinical Operations management, interact with internal stakeholders and external clients to coordinate the accomplishment of business needsRequirements:BS degree or BS degreeRelevant clinical or basic research experience working at an Investigator Site, Sponsor or Clinical Research OrganizationFamiliarity of clinical trial operations, ICH, GCP Guidelines Good working experience in a team environment across multi-functional areasHighly organized, self-motivated, detail-oriented, proactive, and accurateAbility to work with urgency and thrive in a high-energy, fast-paced environmentDemonstrate excellent communication, verbal and written, and interpersonal skillsFluent in written and spoken English and GermanDemonstrate proficiency in MS Office Suite: Word, PowerPoint, Excel, Project ABIOMED is an Equal Employment Opportunity employer. We are committed to the policy of providing equal employment opportunities without regard to race, color, religion, sex, sexual orientation, gender identity, disability or national origin. Über das Unternehmen:Johnson and Johnson

Company DescriptionAbout UbisoftUbisoft’s 21,000 team members, working across more than 30 countries around the world, are bound by a common mission to enrich players’ lives with original and memorable gaming experiences. Their commitment and talent have brought to life many acclaimed franchises such as Assassin’s Creed, Far Cry, Watch Dogs, Just Dance, Rainbow Six, and many more to come. Ubisoft is an equal opportunity employer that believes diverse backgrounds and perspectives are key to creating worlds where both players and teams can thrive and express themselves. If you are excited about solving game-changing challenges, cutting edge technologies and pushing the boundaries of entertainment, we invite you to join our journey and help us create the unknown.About Ubisoft MainzThe teams at Ubisoft Mainz are engineering some of Ubisoft’s biggest blockbusters. Operating from a historic city in the heart of Germany, the studio develops games pushing the limits of the genre like the acclaimed Anno 1800 and lends decades of expertise to AAA co-development projects like Tom Clancy’s Rainbow Six Siege and the upcoming Beyond Good And Evil 2. More information at mainz.ubisoft.com.Job DescriptionFor a yetunannounced project developed at Ubisoft Mainz we are looking for a Game Writer (f/m/d). This new project, not related to the ANNO series, has a strong narrative focus, so it is your opportunity to shine! You would work in such varied areas as dialogue writing, systemic game texts, world building, story, and character development. You will be part of a carefully selected and highly motivated team of developers. Your responsibilities: Write in-game-text and dialogue following form and contentCreate characters and the subsequent text and voice linesCreation and support of the audio bookSupport the conception of narrative conceptsSupport story and world building (lore)Work with internal tools to manage text creation, localization, and version controlLecture and rework 3rd party text contentsCreate additional game text for UI and marketingClosely collaborate with all disciplines inside a focused teamQualificationsWhat you bring:Valid experience as a game, screen, or creative writerExcellent writing skillsNative English language levelA broad area of interest exceeding gamesTeam player with a positive mindsetA superior motivation to create high quality contentBonus:Ability to work with digital text management toolsKnowledge and interest in psychology, philosophy, and historyInterest in literature (e.g. Poe, Lovecraft, Jackson, Maurier) and pop culture (horror)German language skills are a plusWhat to send our way: Your CV, highlighting your education, experience, and skillsA cover letter including your earliest starting date, expected salary and why you would like to join us Please provide samples of your writing/previous work with your application.Additional InformationWhat we offer:Relocation support: We offer financial support in form of a cash allowance and assistance with accommodation search and settle-in support via our relocation partner, for international candidates we offer visa assistance Ubisoft Blue Byte Academy: We offer multiple opportunities for you to discover your full potential and develop yourself in various areas. Guest speakers from the industry, workshops, and access to our training and development platform as well as to our in-house libraryDiscounted and free games: Discount on employee game orders & free Ubisoft games on Ubisoft Connect Hybrid work model: Provides the flexibility to combine working from the studio and your home within GermanyMonthly Mobility Budget: 80€ per month that can be used on bicycle lease, parking spot rental or public transportation ticket Up to 350€ childcare support per child per month Company Pension Scheme: We offer an attractive company pension scheme Gym subsidy: We contribute 50% (up to a maximum amount of 25€) towards the monthly cost of a gym membership of your choice English and German online lessons for free: Good to know: Our main language in the studio is English 26 days paid vacation per year Corporate Benefits web portal: Employee discount program for affiliated retailers, shops, and service providers We offer a highly motivating challenge for team players interested in showing personal initiative in an innovative and international company. If you are passionate about video games and would like to join an industry leader - please apply via our career portal. For further information, please check https://mainz.ubisoft.com/en/Über das Unternehmen:Ubisoft

Curious about the future of event marketing?SpotMe is the enterprise event platform to manage engaging events that help accelerate customer relationships at scale. Trusted by 12,000+ global Fortune 500 business leaders and loved by 10,000,000+ users, brands like J&J, Deloitte, and Red Hat use SpotMe to manage hybrid, virtual, and in-person events with a branded, personalized and compliant experience and get deep data insights that flow into their CRM.Behind the magic stands a curious, diligent, and humble team with over 30 nationalities. A team that feels great pride in the work they do, a team that cares for each other, and a team that is always ready for the next challenge.Mission: Responsible for delivering Virtual, Hybrid and In-person events from kickoff to post-meeting review.Responsible for coordinating internal resources and customer teams for Virtual and Hybrid events creation.Responsibilities:Lead projects following our high-quality standards and best practices to ensure great client experience. Make sure all of the events are executed within the agreed deadlines.Use our powerful Backstage CMS to tailor-make the clients’ apps and to ensure the best participants' experience before, during, and after the event.Be a Backstage subject-matter expert for our customers.Brief and manage the assigned operations team (Live coordinator,Live producer, Onsite coordinator)Requirements & Skills:Fluent in EnglishFluent in German and any another language will be considered a strong advantageExcellent organizational and prioritization skills, always meeting deadlines.Detail-oriented, high-standards achiever without excusesExcellent computer skills and tech-savvinessProficiency with Microsoft packages (PowerPoint, Excel, Word) or Google WorkspaceRequired to travel onsite for up to 3 events per month during busy seasons Eligible to travel internationallyPast experience in an Event Agency, PCO, or other event-related position is a plus.SpotMe recruits, compensates, and promotes regardless of race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, parental status, or veteran status.

Sie arbeiten in einem renommierten, erfolgreichen und bei einem im Markt gefestigten UnternehmenZusammenarbeit: Teamarbeit und ein produktives Miteinander sind Kernwerte des UnternehmensBetriebsklima: Sie arbeiten in einer angenehmen Atmosphäre mit kollegialem ZusammenhaltAbwechslung: Das Aufgabengebiet ist vielfältig und Ihre Ideen und Lösungsvorschläge sind gerne gesehenWir bieten: Weihnachts- und Urlaubsgeld, Arbeitgeber finanzierte Altersvorsorge und einiges mehr an attraktiven Benefits zum Gehalt Unterstützung des Project Manager Web Applications bei der Implementierung, Konfiguration und Weiterentwicklung der relevanten WebanwendungenSupport zu Fragen unserer WebanwendungenDiagnose und Fehlerbehebung von technischen ProblemenEnge Zusammenarbeit mit dem Entwicklungsteam und der ProjektleitungIdentifizierung von Bereichen zur Prozessverbesserung und Abstimmung mit dem Vorgesetzten, um diese umzusetzenBetreuung, Überwachung und Testen unserer WebanwendungenKommunikation mit allen ProjektbeteiligtenDokumentation und Aufbereitung von Supportthemen als FAQ, Dokumentation von LösungswegenErstellen von klar definierten Anforderungen zur Beseitigung von Fehlern oder Einführung neuer FunktionenVerstehen und Weitergeben der Produktvision und der Strategie für unsere Webanwendungen Du besitzt ein abgeschlossenes Studium der Wirtschaftswissenschaften Wirtschaftsinformatik, eine abgeschlossene Ausbildung im IT-Umfeld oder eine vergleichbare QualifikationVerständnis für Prozesse und Zusammen¬hänge zwischen verschiedenen IT-Systemen.Erfahrung in der technischen Entwicklung und im IT-SupportErfahrung in der Konfiguration von Webanwendungen (Produktkatalog, Preise, Rabatte, Zahlungsoptionen, Liefermöglichkeiten, etc.)ERP-Know-how, insbesondere Schnittstellen-Know-how zwischen ERP-Systemen und Webanwendungen ist von VorteilErfahrung mit Ticket-Systemen wie z.B. JiraAusgeprägte Kommunikations- und ProblemlösungsfähigkeitenKonsequentes service- und kundenorientiertes Denken sowie sehr gute KommunikationsfähigkeitenStarke analytische und konzeptionelle FähigkeitenDu findest dich schnell in einem neuen Softwaresystem zurechtKundenorientierung und die Fähigkeit, in einem sich schnell ändernden Umfeld zu arbeitenFließende Deutsch und Englischkenntnisse in Wort und SchriftAndere Sprachen sind von VorteilEine Stellenanzeige von PM-International AG''

Job Description Northvolt has an exciting opportunity to join our team in Heide as a Site Design Interface Coordinator. In joining us you will play an important part in the construction of our large scale European battery factories. As a Site Design Interface Coordinator, you will work in a cross-functional highly motivated team to drive the factory design and maintain and continuously improve the blueprint as the backbone for key building blocks of the large-scale battery factory.You will also support and collaborate with the Northvolt factory programs from the different sites in Europe and Worldwide to deploy and leverage the factory design for a more efficient and speedy delivery. Your responsibilities will range from concept phase up to the end of basic design, and also supporting the site programs during the detail design and execution.The team’s mission is to deliver a digital factory blueprint of a scalable, rapidly deployable, highly efficient world-class battery factory. It constitutes a comprehensive solution with guidelines and tools needed for the establishment of the factory spanning process, equipment, materials, facility, utilities and people.To summarize, Blueprint & Factory Engineering is a highly strategic but also execution oriented and cross-functional team which aids Northvolt in our mission to enable the future of energy.Key responsibilitiesSet the direction and drive technical decisions on the design to ensure that the factory site designs are competitive (cost/performance), modular, easy to ramp up, and possible to operate in a sustainable way.Organize and manage design reviews, construction design packages and deliverables to support all aspects of construction, including scope of work, kick-off, studies, 30-60-90, etc.Capture Lessons Learnt to address critical issues and prevent repeated mistakes while contributing to building a learning organization.Develop & drive standards for key design documents.Enable suitable project delivery methods, like integrated engineering project development, and fast track projects.Perform design option analysis for cost efficiency, constructability, etc.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 Germany 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.Apply with CV in English or your complete LinkedIn profile.Full time employment, fixed salary.Planned starting date is asap.

Job Description We are searching for an experienced and motivated BIM Coordinator in Germany to join our team for a major capital project in Northern Germany. You will be part of the Factory Program team that will drive the planning, purchasing, construction and commissioning of our new battery factory in Heide, Germany. Built in multiple phases over 5+ years the factory represents a multi-billion Euro investment project. Together with your colleagues from the Program team you will be accountable to lead internal and external teams cross-functionally to deliver on company targets and in line with customer expectations.About the jobCoordinate the multi disciplinary design and work together with internal and external stakeholders to provide needed BIM expertise and model support. Key responsibilities include but are not limited to:Collaborate with the multi-discipline engineering team and project stakeholders to ensure optimised BIM delivery and support through all project phases as well as clash Detection and communicationEnsure project compliance with central BIM strategy in assigned scope and quality check data deliverables and project informationRun design review and coordination meetings as well as report Model data to stakeholders, while being able to support in developing BIM assets and templatesSupervise change management and model development within assigned scope and facilitate Constructability reviews with all stakeholdersResponsible for 4D and 5D implementation in assigned scope and support development of ways of working together with internal experts and stakeholdersThe person we are looking for has great communication skills as have constant interaction with team members and external parties such as contractors, vendors, authorities and auditors. You have high work ethic, you are a multi-tasker with strong analytical ability and attention to details as well as critical thinking, and problem-solving skills. You also need to be passionate & purpose driven - as we work for a more sustainable future and have a can do-attitude with an entrepreneurial spirit together with the ability to work well with others in a team environment, as well as independently. We are looking for a driven, caring and structured team member. You are used to a high paced work environment and got good time management skills. Qualities that we cherish are flexibility, sense of quality, friendliness, motivation to take on new challenges, grit and a sense of humor, while being highly organized and result driven. 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.

Job Description We are looking for Technical Project Coordinator - Korean Speaking to join us in our mission to contribute to a greener future. The role is a part of our engineering team based in our gigafactory in Skellefteå. By joining us, you will contribute to building one of the first large scale European battery factories. About the jobKey responsibilities include but are not limited to: •Coordinate project management activities, resources, equipment and information.•Act as the point of contact and communicate project status to all participants•Translation and communication interfacing between Northvolt Engineers, Project Managers and equipment supplier engineers•Work with the Project Manager to eliminate blockers.•Use tools to monitor and report project activities status.•Track assigned tasks with internal teams and external teams-•Ensure standards and requirements are met through conducting quality assurance.•Experience and interest in equipment design, process development and commissioning. 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.

Job Description Northvolt has an exciting job offer for a Project Logistics Manager to join our excellent and passionate team, based in Heide. In joining us you will play an important part from the very start, building Northvolt's Heide Gigafactory. Northvolt will play a significant role in the transformation to a carbon free society. The Project Logistics Manager's primary focus will be to lead, grow and develop a team (Developers, Specialists, Coordinators and interns) who design and implement logistics solutions for heavy process equipment during the construction phases of Northvolt's Gigafactory in Heide. Ensuring team engagement, unity and motivation are essential and strategic planning and resource management to effectively impact operational excellence comes naturally.Secondly, you are an Industrial Project specialist. You understand the importance of planning before the execution kicks in and the sequence of events of a logistical process. The Project Logistics Manager will be responsible for procurement and execution of all land-side logistical activities from port of destination via warehousing to position of installation. QHSSE management is in your DNA and you walk the talk every day, leading by example to ensure the development of safe practices.We:In broad terms, Project Logistics is responsible to secure end to end logistical solutions for process equipment, from vendor to installation with the highest focus on QHSSE, Schedule & Budget.You:First and foremost - you are a hands-on leader. You are a natural when it comes to human interaction, managing a broad scope of activities across a very busy team, spread through multiple locations, geographies and time zones. You have a good feel for people and you know how to, together with them, celebrate good times, as well as pull through dire straits.Generally speaking, you have a high degree of experience within logistical operations, specifically in an industrial projects setting. You are absolutely excellent in multi-tasking and prioritizing. You understand the importance of structure and communication, especially across cultures and time zones, as means to ensure clarity and reach common goals within specific time frames.The role will be based at Northvolt’s Heide facility with regular travels to Stockholm, and Northvolt's production facilities in Europe.Together with the wider Northvolt Project Logistics Team you will:Lead the preparations, planning, co-ordination and execution of landside activities for cargo across multiple transport modes covering last mile, warehousing and last meter requirements,Ensure QHSSE development, implementation, measurement, analysis and optimisation and foster QHSSE culture,Ensure forecasting and plan solutions accordingly,Procure, contract and implement LSP agreements. Measure manage and optimize supplier performanceMeasure team and project performance, implementing actions to drive optimisation,Lead the co-ordination of schedule and budget planning and reporting between internal Northvolt departments,Take a lead role in developing and enhancing operational procedures,Participate in structured and unstructured communication to ensure clarity around next steps and ultimate goals,Continuously improve overall project logistics operations.

Job Description Project Coordinator is within the Engineering Team the responsible person for coordinating projects related to continuous Improvements, commissioning and/or brownfield etc. Project Coordinator manage activities in very close collaboration with the Production Team as well as the Engineering team. Ensuring full project plan is understood and the daily plan is executed upon.Driving the activities on the shop floor and supporting ETT Engineering teams, as well as other affected departments if needed.Coordinates with the neighboring teams like Production, Quality, Maintenance, but also within the ETT Engineering Team.Closely follow the progress of the projects, report progress and successes.Supplier coordination for new equipment installation.

Jetzt bewerben und Zukunftschancen sichern! Unsere Personalvermittlung sucht ab sofort im Auftrag des Kunden: Assistant Housekeeping Manager & Technical Coordinator (m/w/d) in Berlin Ort: Berlin-MitteLage: ZentralArbeitszeit: VollzeitGröße: ca. 5 Standorte, 50-250 Zimmer, Restaurants, Bars, TagungsräumenArt des Betriebes: moderne Hotelgruppe bestehend aus mehreren Boutique Hotels verschiedener Kategorien Ihre Aufgaben Administrative und organisatorische Leitung der Housekeeping Abteilung und regelmäßige Schulung des Personals Notwendige Wartungen / Wartungsverträge beauftragen und überwachen; enge Zusammenarbeit mit technischen Dienstleistern Kontrolle der gereinigten Zimmer, der Etagen, Treppenhäuser und Outlets auf die Qualitätsstandards Erstellung von Reinigungs-, Instandhaltungs-, und Wartungsplänen in Zusammenarbeit mit dem Director of Housekeeping & Engineering Kontrolle des Lagers und Disposition der Artikel, die Prüfung der Wäsche- und Warenlieferungen sowie Durchführen von Inventuren Ihr ProfilErfahrungen im Housekeeping / Hotellerie / Gastronomie sind wünschenswertEngagement und Leidenschafteigenständiger und selbstständiger Arbeitsstilstarke Kommunikation mit Gästen, Mitarbeitern und Vorgesetztengute Deutsch- und Englischkenntnisse in Wort und Schrift Ihre Vorteile Unterstützung bei der Wohnungssuche in Berlin mit einem kostenfreien WG-Zimmer innerhalb der Teams für 2 Monate 28 Urlaubstage, ab dem 3. Jahr 30 Urlaubstage Zukunftsperspektive durch Transfermöglichkeiten innerhalb der Hotelgruppe Zahlreiche monetäre Benefits wie Sachbezüge, Gutscheine oder Geburtstagsgeld Wohlfühl-Care-Paket (u.a. Krankenzusatzversicherung, Gesundheitstag, etc.) Sie möchten wechseln? Das bleibt unter uns! Wir werden nur mit Ihrer Zustimmung den mögliche Arbeitgeber kontaktieren. Telefoninterviews gerne auch nach Feierabend oder am Wochenende. Passt nicht? Kein Problem Die Stellenbeschreibung passt nicht so ganz zu Ihren Wünschen und Vorstellungen? Wir suchen immer Kandidaten und Talente mit Ihren Kenntnissen! Senden Sie uns einfach Ihren aktuellen Lebenslauf mit Lichtbild zu, alles weitere klären wir im Nachgang per Telefon. Unsere Kontaktdaten finden Sie am Ende dieser Ausschreibung. So geht es weiter Wenn Sie bereits bei uns registriert sind und diese Ausschreibung von uns zugeschickt bekommen haben, antworten Sie bitte einfach auf unsere Nachricht. Wenn Sie noch nicht mit uns im Kontakt stehen, bewerben Sie sich bitte direkt online, indem Sie auf \"Jetzt online bewerben\" klicken. Nutzen Sie bei Fragen vorab die Kontaktdaten Ihres Ansprechpartners. Wir vereinbaren nach Prüfung der Unterlagen einen Telefontermin für ein kurzes Interview mit Ihnen. Sie erfahren im Gespräch den konkreten Arbeitgeber hinter dieser Stelle. Bei Interesse stellen wir Sie dort vor. Wenn nicht, werden Ihre Daten natürlich nicht weitergeleitet. Der Arbeitgeber kontaktiert Sie für ein Bewerbungsgespräch; die Anstellung erfolgt dann ebenfalls beim Arbeitgeber direkt. Klingt das gut? Dann bewerben Sie sich jetzt. Wir freuen uns auf Sie! Eine Stellenanzeige von CR Personalvermittlung