Careers
Join us as we strive to make the unprecedented possible
Explore Career Opportunities
Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, will continue to expand and hire across key areas including:
- Biostatistics
- Clinical Development
- Clinical Operations
- Clinical Pharmacology
- CMC
- DMPK
- Medical Affairs
- Program Management
- Quality Assurance
- Regulatory Affairs
- Safety and Pharmacovigilance
- Supply Chain
- Toxicology
We encourage you to explore available opportunities on the Lilly Career site.
Search “Centessa” in the keyword search box.
At Centessa, we embrace our core values in our mission to discover and develop medicines that are transformational for patients. We are leaders, innovators, and entrepreneurs working together to redefine the way medicines are made.
Our Core Values
We seek out innovation. We conduct our work with integrity. We are accountable. We value collaboration.
Innovation
We are bold and courageous
We welcome change
We have a sense of urgency in getting medicines to patients
Integrity
We follow the science and respect the data
We commit to transparent decision making
We are humble
Accountability
We follow through on commitments
We pursue excellence in drug development
We are accountable for our decisions
Collaboration
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We respect all perspectives
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We share information and ideas openly
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We embrace cross functional teamwork
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We leverage other team members and partners
Explore Career Opportunities
- Associate Director, Clinical Quality Assurance
- (Associate) Director, Clinical Science
- Associate Director, Clinical Supply Chain
- Associate Director, Project Management
- Associate Director, Regulatory Project Management
- Associate Project Manager, Drug Development
- CMC Technical Writer (Contract)
- Director, External Quality Control & Stability
- Director, HEOR – Orexin Franchise
- Director, Medicinal Chemistry
- Director, Supplier Quality, Inspection & Audit
- Inventory Control Manager, Supply Chain (contractor)
- Manager, Clinical Supply Chain
- Manager, Product Quality
- Medical Science Liaison (MSL) – North Central
- Senior Advisor, Manufacturing Package Design
- Senior Advisor, Molecular Pharmacology
- Senior Advisor, Regulatory Starting Material
- Senior Clinical Trial Manager (Contract)
- Senior Clinical Trial Specialist (Contract)
- Senior Director, Analytical Development CMC
- Senior Director, DMPK Project Leader
- Senior Director, Drug Product CMC
- Senior Director, Global Medical Affairs
- Senior Director, Global Regulatory Strategy
- Senior Director, Patient Advocacy
- Senior Director, Regulatory CMC
