Fortrea in London seeks a regulatory-focused Study Start-Up Project Manager to lead country-level submissions, approvals and site readiness for a global client-dedicated program.
You will oversee end-to-end regulatory submissions, IRB/IEC interactions, and local documentation, while coordinating with cross-functional teams to meet timelines and budget. This hybrid role offers ownership and visibility in a high-impact area.
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Kent
We are seeking an experienced Hub Submission Manager to join a global regulatory operations team within a highly regulated pharmaceutical environment.
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