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Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company

Remote Job Openings at Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company (5)

Associate Director, Statistical Programming

United States $166K - $242K per year 10+ yrs exp Others

The Associate Director will provide strategic leadership for statistical programming activities and ensure compliance with regulatory standards across clinical trials. They will also manage team members, oversee CRO activities, and collaborate with cross-functional teams to ensure high-quality data reporting.

Associate Project Manager, Drug Development

United States $80000 - $130K per year 2-5 yrs exp Product

The Associate Project Manager provides operational support for drug development programs by maintaining project timelines, budgets, and forecasting within a PPM system. They also assist senior project managers with meeting logistics, status reporting, and monitoring project deliverables.

Senior Director, Clinical Pharmacology

United States $195K - $275K per year 10+ yrs exp Healthcare

The Senior Director will provide strategic leadership for translational clinical pharmacology across the neuroscience pipeline, from early development through registrational programs. They will drive dose selection and optimization by integrating PK, PD, and safety data while representing the company in regulatory interactions.

Medical Science Liaison (MSL) – North Central

United States $175K - $215K per year 2-5 yrs exp Healthcare

The MSL serves as a scientific expert engaging with healthcare professionals and KOLs to translate complex data into clinical insights. They support clinical trial site identification, provide scientific education, and develop compliant medical materials.

Medical Science Liaison (MSL) – South East

United States $175K - $215K per year 2-5 yrs exp Healthcare

The MSL serves as a scientific expert engaging with healthcare professionals and key opinion leaders to translate complex data into clinical insights. They support clinical trial site identification and provide scientific education to investigators and internal teams.