Related skills
pi ich-gcp gmc_registration uk_mhra📋 Description
- Medical Monitoring: review adverse events and safety data.
- Investigator Responsibilities: PI/Sub-Investigator on trials.
- Sponsor Liaison: medical contact for sponsors and safety reviews.
- Protocol Development: contribute to trial design and refinement.
- Therapeutic Area Coverage: support trials across multiple areas.
- Remote-friendly, approx 1 day per week, part-time role.
🎯 Requirements
- Qualified physician with active GMC registration (GP/IM).
- Prior PI experience on clinical trials.
- Clinical trial experience in CRO/pharma/biotech/academic.
- Strong grasp of ICH-GCP and UK/MHRA regs.
- Excellent communicator with sponsors and cross-functional teams.
- Commit to ~1 day/week and on-call rota.
🎁 Benefits
- Competitive senior rate, pro-rated to part-time commitment
- Additional payment for on-call rota participation
- Insurance coverage for all work undertaken
- Remote-friendly, approximately 1 day per week
- Direct collaboration with VP Medical and senior leadership
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