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Senior Director Clinical Development, Stoke-on-Trent
Client:
Advanced Resource Managers
Location:
Stoke-on-Trent, United Kingdom
Job Category:
Other
EU work permit required:
Yes
Job Views:
2
Posted:
22.08.2025
Expiry Date:
06.10.2025
Job Description:
Position: Senior Director, Clinical Development – 37 hours per week - 6 months
This position is responsible for overseeing the medical aspects of clinical trials, ensuring compliance with SOPs, client directives, good clinical practices, and regulatory requirements.
The Senior Director will participate in investigator and sponsor meetings, provide medical consultations, and support business development. Responsibilities include reviewing serious adverse events, safety reports, and other client deliverables.
The role involves managing all medical components throughout the pharmaceutical product lifecycle, ensuring effective execution by the Pharmacovigilance Group in accordance with regulations and ICH guidelines.
The Senior Director will also provide medical consultation to team members, address study-related medical inquiries, and maintain communication with clients and associates. Training on therapeutic areas and study protocols may be provided. Monitoring safety variables such as adverse events and laboratory abnormalities is essential, along with discussing medical concerns with investigators and clinical teams. The role includes assisting in writing and reviewing regulatory documents to ensure medical accuracy.
This is a freelance project, based in any EU country, with a duration of 6 months and potential for extension.
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