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Senior Director Clinical Development, Basingstoke
Client: Advanced Resource Managers
Location: Basingstoke, UK
Job Category: Other
EU work permit required: Yes
Job Views: 2
Posted: 22.08.2025
Expiry Date: 06.10.2025
Job Description:
Senior Director, Clinical Development – 37 hours per week - 6 months
This position is responsible for overseeing the medical aspects of clinical trials. The role ensures compliance with company standard operating procedures (SOPs), client directives, good clinical practices, and regulatory requirements.
The Senior Director will participate in investigator and sponsor meetings, provide medical consultations to clients, investigators, and project teams, and support business development initiatives. Additionally, the position involves reviewing and analyzing serious adverse events from clinical trials, as well as periodic safety reports and other client deliverables.
In this capacity, the Senior Director manages all medical components of contracted tasks throughout the pharmaceutical product lifecycle. It is essential to ensure that tasks assigned to the Pharmacovigilance Group are executed effectively while adhering to relevant regulations and ICH guidelines.
The Senior Director will also provide medical consultation to team members, address study-related medical inquiries, and maintain communication with associates and clients to ensure procedural compliance. Training on therapeutic areas and study protocols may be provided as needed. Furthermore, the Senior Director will monitor safety variables in clinical studies, including adverse events, laboratory abnormalities, and changes in patient medical status. Engaging with principal investigators and clinical teams regarding medical concerns is critical. The role also involves assisting in the writing and review of regulatory documents, ensuring medical content accuracy and comprehensiveness.
This is a freelance project, where you can be based in any EU country. It is a 6-month project with scope for extension.
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