22/03/2024 | Parttime, Fulltime | Organon LLCAt the request of the clinical trials organization personnel. - Provide insights on the scientific gaps, ideas and other topics gathered from scientific exchange to inform areas of interest, development programs, and company strategy. - Support company commercial colleagues by providing on-label or disease state
Save for later12/03/2024 | Fulltime | CV-Library | - £28 / Hour For occasional meetings onsite). Manager, Trial Supplies Management Role Collaborates with internal Global Clinical Supply Chain (GCSC) teams, external Customers & Service Providers Medical to ensure all needs are met. Proactively defines, plans, & communicates the clinical supply chain strategy in support
Save for laterRegister your CV11/03/2024 | Fulltime | Hillingdon | CV-Library | £28 - £32 / Hour Clinical Trial Supplies Management Manager Contract 12 months Location (Hybrid 50% home based and 50% in Uxbridge) Our client is looking for a Trial Supplies Management Manager to create and maintain supply strategies for all investigational products for drug development. The key responsibilities
Save for laterRegister your CV20/03/2024 | Fulltime | Pharma SearchInternational - History - Established in the late 1970's with name changed to Pharmaceutical Research Associates Inc., in 1981 with focus on data management in Virginia, USA. - In 1991, PRA expanded its service offering to include clinical trial management and opened their first European location. - 1996 saw
Save for later19/03/2024 | Fulltime | Medpace, Inc.Europe. Responsibilities - Provide medical management and expertise for clinical trials; - Contribute medical expertise to study reports, regulatory documents, and manuscripts; - Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials
Save for later21/03/2024 | Fulltime | Offenbach am Main, Worms, Fran | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Aschaffenburg, Cambridge, Fran | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Kaiserslautern, Mainz, Rüssels | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Rüsselsheim, Mainz, Wiesbaden | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Aschaffenburg, Cambridge, Worm | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
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