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Senior Director Clinical Development, Cardiff
Client:
Advanced Resource Managers
Location:
Cardiff, 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 participates in investigator and sponsor meetings, provides medical consultations, and supports business development. Responsibilities include reviewing serious adverse events, safety reports, and other deliverables.
The role manages all medical components throughout the pharmaceutical product lifecycle, ensuring effective execution by the Pharmacovigilance Group in compliance with regulations and ICH guidelines.
The Senior Director offers medical consultation, addresses study-related inquiries, maintains communication with team members and clients, and provides training on therapeutic areas and protocols as needed. Monitoring safety variables and discussing medical concerns with investigators are also key duties. Additionally, the role involves 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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