Fortrea is seeking a Study Start-Up Project Manager to lead country-level regulatory submissions, approvals and site readiness for a global, client-dedicated program. The role involves coordination across internal teams, external authorities, and vendors, with a hybrid work model requiring 2-3 days in London.
The ideal candidate has 5+ years in clinical research with strong start-up/regulatory exposure and a solid understanding of local regulatory environments.
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Client-Dedicated Study Start-Up Lead 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.
