ADME Project Leadership for Genetic Medicines

BioSpace; Boston (MA); On-site; USD 194,000 - 339,000; Full time

Benefits offered by this job

Company bonus

Comprehensive benefits package

401(k) retirement plan

Job summary

Lilly is seeking an experienced ADME/DMPK scientist for our Boston campus to lead ADME studies supporting preclinical and clinical genetic medicines. You will integrate ADME/PKPD data with discovery chemistry and biology to inform design, delivery, and regulatory strategies.

We value strong problem-solving skills, global collaboration, and the ability to communicate complex data to diverse teams. This is a full-time, on-site role in Boston, MA with a competitive benefits package.

Qualifications

• Ph.D. or equivalent in a relevant scientific field with substantial ADME/PKPD experience.
• Strong problem-solving skills and ability to test ADME hypotheses across modalities.
• Experience integrating ADME/PKPD data with discovery biology and chemistry data.

Responsibilities

• Lead ADME studies to support preclinical and clinical development of genetic medicines.
• Integrate ADME, PK and PK/PD endpoints with discovery data to guide design and delivery strategies.
• Design and interpret hypothesis-driven studies addressing TK and toxicokinetics questions.
• Collaborate cross-functionally and with regulatory teams on global submissions.
• Prepare ADME portions of regulatory documents and interact with authorities.
• Mentor colleagues and foster cross-level coaching and collaboration.
• Communicate clearly to influence teams and stakeholders.

Skills

Learning agility

ADME/PKPD knowledge

Data integration across in silico/in_v

Education

PhD in Biochemistry/Biology/Pharmacokinetics/Bioengineering/Pharmacology

5+ years pharma/biotech ADME/PKPD experience

Tools

PK/PD modeling

Bioanalytical methods (LC/MS, PCR)

Job description

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.

Our ADME team is seeking a scientist with an interest in the discovery and clinical development of genetic medicines, including gene editing, gene therapy, siRNAs, ASOs, and other emerging modalities. We develop transformative therapeutics that address the underlying causes of disease across a wide range of therapeutic areas. We welcome applicants with strong problem-solving skills and innovative thinking to join our growing Boston campus team.

Lilly's ADME team collaborates with biologists, chemists, engineers, and other R&D functions across all stages of discovery and development, sharing learning and responsibility for advancing next-generation genetic therapies. We foster professional growth and welcome motivated, collaborative scientists who want to help improve patient outcomes globally.

A High-quality Candidate Will Demonstrate The Following

• High learning agility and the ability to articulate and efficiently test ADME and PK/PD hypotheses for complex novel molecules
• Strong working knowledge in fundamental pharmaceutics, pharmacokinetics/pharmacodynamics, and ADME principles - especially as they relate to genetic medicine therapeutic modalities
• Ability to interrogate diverse data (e.g., in silico, in vitro, in vivo) to derive mechanistic understanding of drug action and ADME/DMPK characteristics
• Understanding of pharmaceutical regulatory guidance and expectations

Lilly seeks a skilled ADME / DMPK scientist who will:

• Lead and innovate in a multidisciplinary team environment with primary responsibility for ADME studies to support preclinical and clinical development of the Lilly genetic medicines portfolio
• Integrate ADME, PK and PK/PD endpoints with discovery chemistry and biology data to guide preclinical drug design, optimization, and delivery strategies.
• Design, implement, and interpret hypothesis-driven studies to inform key ADME, PK/PD, and toxicokinetic (TK) questions
• Collaborate and innovate with cross-functional and interdisciplinary colleagues
• Lead the preparation of ADME portions of regulatory communications and documents to support clinical development, new drug applications, and line extensions and interact with global regulatory authorities
• Mentor and build relationships with colleagues at all levels through coaching and support
• Strong written and verbal communication skills, with the ability to constructively lead and influence teams

Basic Requirements

• Ph.D. in Biochemistry/Biology/Pharmacokinetics/Bioengineering/Pharmacology or a related scientific field
• Greater than five years of experience as a scientist in a pharmaceutical and/or biotechnology company in a role related to ADME or PK/PD

Additional Skills/Preferences

• Knowledge of DMPK and/or bioanalytical considerations for gene editing and/or gene therapy modalities
• Experience with PK/PD modeling and simulation
• Experience with targeted delivery and biodistribution of oligonucleotides and/or gene therapies
• Understanding of and experience with PCR, immunoassay, and/or LC/MS bioanalytical methodology

Additional Information

This is a full-time position located in Boston, MA.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $193,500 - $338,800

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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