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At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life‑changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
Responsibilities
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- Site identification and qualification.
- Comprehensive site management activities to ensure timely delivery of enrolment readiness, trial recruitment/enrolment and database locks; inclusive of performance management and issue mitigation,
identification and resolution.
- Ensures site and country‑level inspection readiness at all times.
- Understanding local treatment paradigms and standard of care to support targeted feasibility and strategic allocation of trials as required.
- Vendor oversight for site monitoring activities at site/country level.
- Establishes and develops strong professional relationships with active/potential clinical investigators to expand/maintain clinical research partnership opportunities and provide an unparalleled experience for participation in Lilly clinical trials.
- Development of strategic institutional/site relationships to optimize the delivery of clinical trial programs; including across therapeutic areas where applicable.
- Travel required (50‑75%).
Requirements
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- Bachelor’s degree or equivalent in a scientific or health‑related field.
- Minimum of 5 years experience in the pharmaceutical industr
📌 Clinical Research Lead (Madrid)
🏢 Eli Lilly
📍 Madrid
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