We are seeking a Strategic Feasibility Lead to join a global clinical operations team. This high-impact role focuses on the front end of clinical trial planning, from early feasibility to country and site selection, shaping the success of global Phase 1 - 3 clinical programs.
You will collaborate with internal stakeholders and CRO partners to deliver data-driven feasibility strategies, optimize recruitment, and select high-performing sites worldwide. This role is perfect for someone who thrives in a matrix, global environment and enjoys leading strategic initiatives with tangible impact.
What You’ll Do
- Lead and execute feasibility strategy for global clinical trials, collaborating with CROs and internal teams
- Analyze internal and external data (including Citeline) to make actionable recommendations for study planning and site selection
- Forecast recruitment and ensure timely delivery of clinical trials
- Mentor and share best practices with other feasibility team members
- Contribute to developing in-house feasibility tools and methodologies
- Partner with cross-functional stakeholders including clinical program directors, site managers, and patient engagement teams
- Travel as needed (up to 10%)
Who We’re Looking For
- Minimum 4 - 5 years as a lead in feasibility / site selection in Pharma (CRO experience considered if aligned with pharma-facing feasibility work)
- Hands-on experience with Citeline or similar clinical trial intelligence tools
- Global trial experience including US site selection (Europe-only experience is insufficient)
- Experience across Phase 1–3 clinical trials
- Strong analytical, communication, and stakeholder management skills
- Ability to work independently and thrive in a matrix/global environment
Education: Bachelor’s degree required (advanced degrees a plus)