Senior Clinical Scientist - single client dedicated
ICON · Reading, UK +2 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
ICON seeks a Senior Clinical Scientist to lead clinical development programs and early-phase studies, designing and conducting trials that evaluate treatment safety and efficacy. The role involves strategic oversight, protocol development, regulatory submissions, and cross-functional collaboration across multiple therapeutic areas.
What they're looking for
- PhD, PharmD, or MD degree with 5+ years' experience in early development or clinical pharmacology
- Alternatively, BS/MS degree with 10+ years' relevant experience
- Early phase/Phase I clinical trial experience required
- Critical analytical skills and ability to develop creative solutions
- Experience in clinical pharmacology, immunology, or oncology preferred
- Legal right to work in UK, Spain, or Poland
What you'll be doing
- Provide strategic leadership for clinical programs supporting early development and pharmacology initiatives
- Author, review, and approve clinical protocols, analysis plans, study reports, and regulatory submissions
- Execute clinical and pharmacology studies in collaboration with Clinical Operations and physicians
- Develop program strategy for assigned compounds, including clinical development plans
- Draft and review regulatory documents including INDs, Investigator Brochures, and Health Authority submissions
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.