Therapeutic Analytics Lead – Single Sponsor

Are you a clinical operations professional with a passion for feasibility and strategic planning in global trials?

We are seeking a Therapeutic Analytics Lead (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

As a Therapeutic Analytics Lead , you will drive end-to-end feasibility and strategic allocation planning across global trials. Your key responsibilities include:

Feasibility Leadership – Conduct early viability, pre-IMB, and trial-level feasibility assessments. Lead survey analysis and consolidate insights to inform recommendations on site selection, patient enrolment and feasibility, ensuring a cohesive data insights narrative.

Strategic Allocation & Scenario Planning – Validate allocation strategies using internal/external data and tools like Footprint Optimizer (FPO). 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

Please note this role is not eligible for the UK visa sponsorship.

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

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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