📍 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

Learn more about our EEO & Accommodations request here.