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Study ‑Up Project Manager – Client Dedicated

Job in Maidenhead, Berkshire, SL6, England, UK
Listing for: FTMAI Fortrea Development Ltd
Part Time position
Listed on 2026-10-04
Job specializations:
  • Healthcare
Salary/Wage Range or Industry Benchmark: 65000 - 90000 GBP Yearly GBP 65000.00 90000.00 YEAR
Job Description & How to Apply Below
Position: Study Start‑Up Project Manager – Client Dedicated

London | 2-3 days onsite (hybrid)

Are you a regulatory-focused Study Start-Up expert who thrives on ownership and compliance? We're looking for a Study Start-Up PM to lead country-level submissions, approvals and site readiness for a global, client-dedicated program.

What you'll own
  • Oversight of end-to-end regulatory submissions and approvals in line with ICH-GCP, UK/local regulations, and internal quality standards
  • IRB/IEC and Regulatory Authority interactions, including amendments and approvals
  • Development and oversight of local regulatory documentation (ICFs, translations)
  • Accountability for regulatory compliance, timelines, and country commitments during start-up and close-out
  • Coordination with CRM, CTC, CRA, Finance, and Legal to deliver submissions, budgets, CTRAs, and local milestones
  • Close collaboration with Headquarters to align country timelines
  • Oversight of site readiness, local vendors, and country-level processes
  • Management of clinical and ancillary supplies, import/export, archiving, retention, and insurance processes
  • Maintenance of country data in clinical and finance systems
  • Acting as a regulatory SME, supporting process improvement, best-practice sharing, and mentoring
What we're looking for
  • 5+ years' experience in clinical research with strong study start-up/regulatory exposure
  • Solid knowledge of local regulatory environments and approval processes
  • Ability to work independently, manage multiple protocols, and mitigate regulatory risk
  • Strong stakeholder-management and influencing skills
  • Bachelor's degree in Life Sciences, Healthcare, Business, or related field
Why this role?
  • High-impact regulatory leadership at the most critical study phase
  • Client-dedicated model with real ownership and visibility
  • Hybrid working model with 2-3 days per week in London

At Fortrea, we're all about turning the "impossible" into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job - it's a journey of making the exceptional possible, every day.

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