Clinical Operations Program Manager (Global Feasibility)

Single Sponsor

We are seeking a Clinical Operations Program Manager (Global Feasibility) to join our Single Sponsor Department. In this role you will lead early viability, feasibility, allocation, and site selection activities to support global clinical development programs.

What We’re Looking For

• ✅ 4–5 years of global feasibility experience in clinical trials
• ✅ Strong understanding of clinical trials, medical terminology and regulatory guidelines
• ✅ Strong analytical skills and strategic planning experience, including scenario planning and risk management
• ✅ Excellent communication and stakeholder engagement abilities
• ✅ Proficiency in feasibility dashboards and data‑driven decision‑making
• ✅ Fluency in English and a Bachelor’s degree in Life Sciences, Public Health, Statistics, Data Sciences or related field (prefered)
• ✅ Excel expertise, ability to analyse data in large databases

What You’ll Do

• Feasibility Leadership – Conduct early viability, pre‑IMB, and trial‑level feasibility assessments. Lead survey analysis and consolidate insights for site selection, patient enrolment and feasibility recommendations.
• Strategic Allocation & Scenario Planning – Validate allocation strategies using internal/external data and tools such as Footprint Optimizer. Develop evidence‑based timelines and risk mitigation plans.
• Stakeholder Engagement – Prepare briefing materials, training resources, and coordinate cross‑functional meetings. Track actions and deliverables.
• Portfolio & Risk Management – Support portfolio tracking, tollgate reviews, and risk presentations. Draft SPF overviews and ensure compliance with internal systems (e.g., IMPACT, CREDI/Subway).
• Operational Excellence – Manage feasibility documentation, pricing assumptions, and logistics for team meetings. Ensure quality handover to study teams.

What You’ll Deliver

• Feasibility excellence across global trials
• Data‑driven allocation and site selection strategies
• Scenario planning and risk mitigation outputs
• Stakeholder‑ready dashboards and briefings
• Compliance with internal systems and documentation standards

This is an exciting opportunity to play a critical role in shaping global clinical trial strategy. If you’re ready to bring your feasibility expertise to a high‑impact role with a leading sponsor, we’d love to hear from you!

Please note: due to sponsor requirements for the role only candidates based in the listed location(s) will be considered. Any applications from candidates based outside of these locations will not be considered.