Related skills
clinical trials pi ich-gcp regulatory compliance protocol development📋 Description
- Medical Monitoring: review safety data and protocol deviations.
- Investigator Responsibilities: act as PI or Sub-Investigator on trials.
- Sponsor Liaison: medical contact for sponsors and safety reviews.
- Protocol Development: contribute to protocol design and refinement.
- Therapeutic Area Coverage: support trials across multiple domains.
- Part-time role (~1 day per week) within Lindus Health Medical function.
🎯 Requirements
- Qualified physician with active medical license in Family Medicine or Internal Medicine
- Prior experience as Principal Investigator (PI) on clinical trials
- Clinical trial experience from CRO, pharma, biotech or academic environments
- Strong knowledge of ICH-GCP guidelines and UK/MHRA regulatory requirements
- Excellent communicator with sponsors and cross-functional teams
- Commit to ~1 day per week and participate in on-call rota
🎁 Benefits
- Insurance coverage for all work undertaken on behalf of Lindus Health
- Remote-friendly, approximately 1 day per week
- Direct collaboration with our VP Medical and senior leadership team
- Flexible, high-impact role that complements other commitments
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