Location: Ahmedabad
Department: Clinical Operations / Feasibility
Reporting To: Head Clinical Operations
Job Summary
End-to-end feasibility activities for clinical trials with a strong focus on oncology studies. The role involves delivering high-quality, data-driven feasibility assessments, supporting business development proposals, and providing strategic inputs for study planning, site selection, and country strategy.
Professionals with a background in Clinical Research Associate (CRA) roles, including onsite monitoring experience, are encouraged to apply.
Key Responsibilities
Feasibility Strategy & Execution
- Lead topline and detailed feasibility assessments for oncology and other clinical studies.
- Analyze patient availability, site capabilities, and operational feasibility across regions.
- Provide data-driven recommendations for site and country selection.
Stakeholder Management
- Act as a key liaison between Clinical Operations (CO), Business Development (BD), Medical Writing (MW), and other internal teams.
- Ensure alignment of feasibility outputs with proposal strategies and client expectations.
Database & Insights Management
- Develop and maintain feasibility databases (investigator/site intelligence, historical study data).
- Enhance feasibility questionnaires and surveys using data insights and past learnings.
Proposal & Study Planning Support
- Support bid defense and proposal development within tight timelines.
- Provide critical inputs including:
- Enrollment projections
- Study start-up timelines
- Budget assumptions
- Operational risks and mitigation strategies
Timeline & Quality Management
- Ensure adherence to feasibility timelines aligned with BD and client requirements.
- Deliver accurate, high-quality feasibility reports.
- Proactively flag risks and delays to stakeholders.
Site & Investigator Engagement
- Maintain robust relationships with investigators, oncology sites, and internal stakeholders.
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