Fortrea in London is seeking a Study Start-Up PM to lead country‑level submissions, approvals and site readiness for a global client‑dedicated program. You will own end‑to‑end regulatory submissions and ensure compliance with ICH‑GCP, UK/local regulations and internal quality standards.
The role requires 5+ years in clinical research with study start‑up/regulatory exposure, strong stakeholder management, and the ability to work independently in a hybrid London setting with 2–3 days on‑site.
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Regulatory Start-Up Lead — Hybrid London in Maidenhead employer: Fortrea
Fortrea is an exceptional employer that offers a rewarding and meaningful work environment, particularly for Senior Technical Designers. With a strong support network, flexible working solutions, and a commitment to employee growth, you will thrive in a collaborative workspace that values diversity and inclusion. Enjoy competitive compensation packages and the opportunity to make a significant global impact while maintaining a genuine work-life balance.
