Study Start‑Up Project Manager – Client Dedicated

Fortrea · Maidenhead, UK

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Clinical OperationsFull timeCompany career page

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Role summary

Fortrea seeks a Study Start-Up Project Manager to lead regulatory submissions, approvals, and site readiness across country-level operations for a dedicated clinical program. The role combines regulatory compliance oversight with cross-functional coordination and vendor management in a hybrid London-based position.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Phenom, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-03 (originally posted 2026-10-03). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

5+ years clinical research experience with study start-up and regulatory focus
Knowledge of local regulatory environments, approval processes, and ICH-GCP standards
Ability to manage multiple protocols independently and mitigate regulatory risk
Strong stakeholder management and cross-functional influencing skills
Bachelor's degree in Life Sciences, Healthcare, Business, or related field

What you'll be doing

Oversee end-to-end regulatory submissions, IRB/IEC interactions, and authority approvals
Develop and maintain local regulatory documentation including informed consent forms and translations
Coordinate with clinical, finance, legal, and vendor teams on submissions, budgets, and milestones
Manage site readiness, clinical supply chains, import/export, and archiving processes
Serve as regulatory subject matter expert supporting process improvement and team mentoring

Privacy & handoff

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