Fortrea

Study Start‑Up Project Manager – Client Dedicated

United Kingdom · Work style not stated · Full time

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About the role

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  • EmployerFortrea
  • LocationUnited Kingdom
  • Work styleWork style not stated
  • Employment typeFull time
  • Employer posted

📍 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
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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

Learn more about our EEO & Accommodations request here.

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ROLIVA currently lists 135 open roles like this in United Kingdom.

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At a glance

  • Employment typeFull time
  • Employer posted
  • Added to ROLIVA
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