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Quality in clinical development is a matter of operational resilience as much as regulatory mandate. This role serves as a GCP Auditor within our Research & Development Quality audit program, responsible for executing the global audit
Role: Regulatory Associate – CTA Contract: 12-month rolling Office- Maidenhead (hybrid) – 3 days on site SRG are partnered with a global biopharmaceutical company with focus and capabilities to address some of the world’s greatest health challenges.
Regulatory Consultant – Clinical Trial Strategy & Submissions Location: Maidenhead - 3 days a week on site – Tues, Wed, Thurs Contract: 12 months We are currently seeking an experienced Regulatory Consultant to join a Clinical Trial