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Senior Director Clinical Development, Crawley, West Sussex
Client:
Advanced Resource Managers
Location:
Crawley, West Sussex, United Kingdom
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, 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, support business development, review serious adverse events, and analyze safety reports and client deliverables.
The role involves managing all medical components of contracted tasks throughout the pharmaceutical product lifecycle, ensuring effective execution by the Pharmacovigilance Group while adhering to regulations and ICH guidelines.
The Senior Director will provide medical consultation, address study-related inquiries, maintain communication with associates and clients, and may provide training on therapeutic areas and protocols. Monitoring safety variables in clinical studies and discussing medical concerns with investigators are also key responsibilities. Additionally, the role includes assisting in writing and reviewing regulatory documents for accuracy and comprehensiveness.
This is a freelance project, based in any EU country, with a duration of 6 months and potential for extension.
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