Fortrea seeks a regulatory-focused Study Start-Up PM to lead country-level submissions, approvals and site readiness for a global client-dedicated program in London. 2-3 days onsite in hybrid model.
You will own end-to-end regulatory submissions, IRB/IEC interactions, local documentation, and alignment with HQ on timelines, budgets and local milestones, ensuring compliance and on-time delivery.
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Hertfordshire
An excellent opportunity has arisen for an experienced Clinical Study Start Up Lead to join one of our longstanding clients, a leading global…
Welwyn Garden City, Hertfordshire
Role: Clinical Study Start Up Lead Location: Welwyn Garden City (Hybrid, 2-3 days in office per week) Hours: Full-time Contract: 6 months, Inside…
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