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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Global Study Start-Up Lead (Hybrid London) in Maidenhead employer: FTMAI Fortrea Development Ltd
Fortrea is an exceptional employer that fosters a collaborative work environment, where teamwork and dedication to patient service are at the forefront. With a hybrid working model in London, employees benefit from flexibility while gaining invaluable experience in complex oncological trials, alongside opportunities for professional growth in regulatory and TMF expertise. Join us to be part of a mission-driven team that values your contributions and supports your career development.
Contact Details:
FTMAI Fortrea Development Ltd Recruitment Team
