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Senior Director Clinical Development, Wakefield
Client: Advanced Resource Managers
Location: Wakefield, United Kingdom
Job Category: Other
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EU work permit required: Yes
Job Views:
2
Posted:
22.08.2025
Expiry Date:
06.10.2025
Job Description:
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, review serious adverse events, and support business development initiatives. The role involves managing all medical components throughout the pharmaceutical product lifecycle, ensuring effective execution of tasks 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, communicate with associates and clients, and may provide training on therapeutic areas and protocols. Monitoring safety variables, discussing medical concerns with investigators, and reviewing regulatory documents are also key responsibilities.
This is a freelance project, based in any EU country, lasting 6 months with potential extension.
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