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Clinical Project Manager (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Support
Projektbeschreibung
REFERENZNUMMER:
275749/11
IHRE AUFGABEN:
-Be involved in all aspects of trials, working closely with and also providing regular updates to the Global Trial Manager
-Liaise with key stake holders e.g. Regulatory, Clinical Trial Supplies, Data Management, Quality Assurance, Legal, Finance etc. for study deliverables
-Ensure trial conduct in adherence to GCP, company SOP, local guidelines and policies, e.g. collaborate with CRAs on site selection and setup, patient recruitment and also data collection
-Participate in investigator meetings and training of CRAs and assisting CRA with addressing study related questions from investigators
-Ensure collection and approval of essential documents and also timely delivery of study supplies for study commencement
-Collaborate regularly with service providers in relation to Central Labs, IMP Management via IVRS to support and address study related issues affecting allocated countries
-Responsible for direct management of CRO, ensuring all delegated tasks are executed per GCP, Company SOP and local laws, within agreed timelines and budget
IHRE QUALIFIKATIONEN:
-Solid experience in clinical trial management
-Solid knowledge in vendor management and budgeting
-Proven field monitoring experience preferred
-Good overview of clinical trial process
-Experience in executing a wide range of trial activities from initiation to study report
-Experience working in a global matrix environment
-Fluent English language skills
WEITERE QUALIFIKATIONEN:
Clinical project manager
275749/11
IHRE AUFGABEN:
-Be involved in all aspects of trials, working closely with and also providing regular updates to the Global Trial Manager
-Liaise with key stake holders e.g. Regulatory, Clinical Trial Supplies, Data Management, Quality Assurance, Legal, Finance etc. for study deliverables
-Ensure trial conduct in adherence to GCP, company SOP, local guidelines and policies, e.g. collaborate with CRAs on site selection and setup, patient recruitment and also data collection
-Participate in investigator meetings and training of CRAs and assisting CRA with addressing study related questions from investigators
-Ensure collection and approval of essential documents and also timely delivery of study supplies for study commencement
-Collaborate regularly with service providers in relation to Central Labs, IMP Management via IVRS to support and address study related issues affecting allocated countries
-Responsible for direct management of CRO, ensuring all delegated tasks are executed per GCP, Company SOP and local laws, within agreed timelines and budget
IHRE QUALIFIKATIONEN:
-Solid experience in clinical trial management
-Solid knowledge in vendor management and budgeting
-Proven field monitoring experience preferred
-Good overview of clinical trial process
-Experience in executing a wide range of trial activities from initiation to study report
-Experience working in a global matrix environment
-Fluent English language skills
WEITERE QUALIFIKATIONEN:
Clinical project manager
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges