Senior Director, DMPK Project Leader

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. 

Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders. Centessa’s lead investigational candidate – cleminorexton (formerly ORX750) – is being developed for narcolepsy type 1, narcolepsy type 2, and idiopathic hypersomnia. Centessa's OX2R agonist portfolio includes additional clinical and preclinical-stage assets with potential utility across a broader range of neurological, neurodegenerative, and neuropsychiatric conditions. Headquartered in Boston, Massachusetts, Centessa was recognized as aGreat Place to Work® in 2026.

Description of Role 

Senior Director, DMPK Project Leader ensures delivery of all DMPK related activities working collaboratively as part of a cross-functional program team. These include nonclinical PK experiments, in vitro ADME, biotransformation studies, bioanalytical and toxicokinetic analysis. This role supports understanding pharmacokinetic, toxicokinetic, and ADME principles to enable progression of drug candidates across the portfolio.  A qualified candidate will have previous experience in PK modeling ideally for CNS drug candidates and a basic understanding of vital ADME properties for CNS drug candidate progression. Furthermore, a qualified candidate will have end-to-end experience in drug discovery and development includingNDA submission; will be able to partner with both discovery and development teams to enable the identification of lead candidates with optimal DMPK properties for progression into nonclinical development and the progression of lead candidates into clinical development.   

Key Responsibilities 

• Lead thefiling ofNDAs for DMPK 

• Deliver high-quality DMPK input and data to projects withinestablished timelines  

• Utilize knowledge of DMPK to support/influence compound profiling, projectprogression and project strategy 

• Proactively calculate PK and toxicokinetic parameters, estimate safety margins and report results and interpretations to project teams and internal governance bodies 

• Lead, coordinate, and engage with DMPK colleagues, clinical pharmacologists, and toxicologists in project related activities 

• Prepare clear presentations related to the above for internal governance bodies 

Qualifications 

• Ph.D. inPharmaceutical Sciences,Pharmacology or a related field 

• Minimum of10 years of industry experience in a biotech or pharmaceutical setting 

• Expert in DMPK sciences with knowledge of drug discovery and development processes 

• Strong analytical and problem-solving skills 

• Experience inDMPKproject leadership 

• Previous work in the discovery and/or development of CNS drug candidates  

• Experience with regulatory submissions including NDAs for small molecules 

• Knowledge, experience, andproficiency in supporting GLP-compliant studies 

• Good knowledge of all DMPK assays including the useofin silico tools for PK prediction 

• Proficiency with PhoenixWinNonlinand other software forNCA and PK modelingin small molecule drugdiscovery and development 

• Demonstrated ability to work cross-functionally and communicate scientific findings clearly and effectively 

• Collaborative mindset andoperates with a sense of urgency 

• Strong, proactive communication skills 

Work Location 

TheSenior Director, DMPK Project Lead role based in the US, with occasional travel.

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Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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