Job Title: Director of Clinical Development - 6-month contract
Client:
Advanced Resource Managers
Location:
Cambridge
Job Category:
Other
EU Work Permit Required:
Yes
Job Views:
1
Posted:
22.08.2025
Expiry Date:
06.10.2025
Job Description:
The primary role involves overseeing medical aspects of clinical trials to ensure compliance with SOPs, client directives, good clinical practices, and regulatory standards. Responsibilities include attending and presenting at investigator and sponsor meetings, providing medical consultations, supporting business development, conducting medical reviews of serious adverse events, and evaluating safety reports such as PBRER, PSUR, and DSUR.
The director manages all medical components throughout the pharmaceutical product lifecycle, ensuring tasks are executed according to regulations and ICH guidelines. The role includes providing medical consultation, monitoring safety variables, discussing safety concerns with investigators and clients, and assisting in the writing and review of clinical and regulatory reports.
Requirements include a medical degree (MD or equivalent), with an active medical license preferred. Candidates should have at least one of the following: clinical experience in a relevant specialty (2+ years), clinical trial experience in CRO or pharma (1-2 years), or experience in safety/pharmacovigilance (2+ years).
If interested, please email [emailprotected] for more details.
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