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Adme Dmpk Jobs (NOW HIRING)

Propose ADME/PK, biodistribution and PK-PD approaches at team discussions of high impact on project progression. * Manage consultants and vendors to support DMPK studies. * Partner with the discovery ...

Propose ADME/PK, biodistribution and PK-PD approaches at team discussions of high impact on project progression. * Manage consultants and vendors to support DMPK studies. * Partner with the discovery ...

Senior Scientist, DMPK

Cambridge, MA · On-site

$130K - $150K/yr

Propose ADME/PK, biodistribution and PK-PD approaches at team discussions of high impact on project progression. * Manage consultants and vendors to support DMPK studies. * Partner with the discovery ...

Lead the Translational IND- and NDA-enabling ADME work; characterize the ADME properties of molecules and collaborate to establish in vitro to in vivo correlations; ensure that all DMPK studies and ...

Lead the Translational IND- and NDA-enabling ADME work; characterize the ADME properties of molecules and collaborate to establish in vitro to in vivo correlations; ensure that all DMPK studies and ...

This includes supporting research operations in areas such as chemistry synthesis/invitro biology/reagent provision, ADME/DMPK services, and operational support for PO generation, finance and budget ...

Lead the Translational IND- and NDA-enabling ADME work; characterize the ADME properties of molecules and collaborate to establish in vitro to in vivo correlations; ensure that all DMPK studies and ...

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Adme Dmpk information

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$45K

$128.4K

$232.5K

How much do adme dmpk jobs pay per year?

As of Jul 28, 2026, the average yearly pay for adme dmpk in the United States is $128,367.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,000.00 and $188,500.00 per year, depending on experience, location, and employer.

What jobs can I do with clinical pharmacology?

With a background in clinical pharmacology, you can pursue roles such as clinical research scientist, pharmacovigilance specialist, regulatory affairs associate, or medical affairs professional. These positions often require knowledge of drug development, regulatory guidelines, and data analysis, and may involve working in pharmaceutical companies, research organizations, or healthcare settings.

What are ADME DMPK scientists?

ADME DMPK scientists specialize in understanding how drugs are Absorbed, Distributed, Metabolized, and Excreted (ADME) in the body, as well as evaluating Drug Metabolism and Pharmacokinetics (DMPK). Their role is crucial in drug discovery and development, as they design and perform experiments to predict a drug's behavior in humans, assess its safety, and optimize its efficacy. By analyzing how drugs interact with biological systems, they help researchers and pharmaceutical companies select the most promising drug candidates for further development.

What is ADME in drug development?

In drug development, ADME refers to Absorption, Distribution, Metabolism, and Excretion, which are key pharmacokinetic processes that determine how a drug behaves in the body. ADME studies help assess a drug's safety, efficacy, and optimal dosing, often involving laboratory experiments and modeling. Professionals in ADME DMPK roles analyze these processes to support drug candidate selection and development.

What are the key skills and qualifications needed to thrive as an ADME DMPK scientist, and why are they important?

To excel as an ADME DMPK scientist, you need a solid background in pharmacokinetics, drug metabolism, and analytical chemistry, typically supported by an advanced degree in a relevant scientific field. Expertise in bioanalytical tools such as LC-MS/MS, in vitro/in vivo assay development, and experience with data analysis software like WinNonlin are commonly required. Strong problem-solving abilities, attention to detail, and effective communication are valuable soft skills in this role. These competencies are essential for generating reliable data, informing drug development decisions, and collaborating within multidisciplinary project teams.

What is the DMPK department in pharma?

The DMPK (Drug Metabolism and Pharmacokinetics) department in pharma focuses on studying how drugs are absorbed, distributed, metabolized, and excreted in the body. Professionals in this department analyze drug behavior to optimize efficacy and safety, often using laboratory techniques and pharmacokinetic modeling. The role requires knowledge of biochemistry, pharmacology, and relevant regulatory guidelines.

What are some common challenges faced by professionals working in ADME DMPK roles, and how can they be addressed?

Professionals in ADME DMPK (Absorption, Distribution, Metabolism, Excretion, and Drug Metabolism and Pharmacokinetics) often encounter challenges such as interpreting complex biological data, keeping up with evolving regulatory requirements, and collaborating across multidisciplinary teams. Adapting quickly to new analytical technologies and effectively communicating findings to both scientists and non-scientists are also crucial. These challenges can be addressed by ongoing professional development, active participation in cross-functional meetings, and leveraging mentorship from experienced colleagues to stay current with best practices and regulatory expectations.

What does DMPK mean in pharma?

In the pharmaceutical industry, DMPK stands for Drug Metabolism and Pharmacokinetics, which involves studying how a drug is absorbed, distributed, metabolized, and excreted in the body. For an Adme Dmpk role, professionals typically analyze these processes to support drug development and optimize dosing strategies using laboratory and modeling tools.
More about Adme Dmpk jobs
What states have the most Adme Dmpk jobs? States with the most job openings for Adme Dmpk jobs include:
Infographic showing various Adme Dmpk job openings in the United States as of July 2026, with employment types broken down into 98% Full Time, and 2% Contract. Highlights an 88% In-person, 5% Hybrid, and 7% Remote job distribution, with an average salary of $128,367 per year, or $61.7 per hour.
ADME Project Leadership for Genetic Medicines

ADME Project Leadership for Genetic Medicines

Eli Lilly and Company

Boston, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago


Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 63 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical


Job description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

Our diverse ADME team is seeking a dedicated scientist with an interest in the discovery and clinical development of genetic medicines, including siRNAs, ASOs, mRNAs, gene editing, and gene therapy. We are committed to advancing scientific boundaries to develop transformative therapeutics that address the underlying causes of diseases across a wide range of therapeutic areas. Applicants with strong problem-solving abilities and innovative thinking are encouraged to apply to join our team at the expanding Boston campus.

Lilly's agile ADME team collaborates closely with biologists, chemists, engineers, and various other R&D functions to deliver novel genetic medicines to patients. Team members support each other through shared learning and collective responsibility for all stages of the discovery and development process for next-generation genetic therapies. We strive to foster professional growth while advancing science to provide safe and effective new treatments to patients. Prospective candidates who are motivated, collaborative scientists interested in spearheading innovation in genetic medicine therapies are invited to connect with us and contribute to improving patient outcomes globally.

A high-quality candidate will demonstrate the following:

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

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
  • Design, implement, and interpret hypothesis-driven studies to inform key ADME, PK/PD, and toxicokinetic (TK) questions
  • Integrate ADME, PK and PK/PD endpoints with discovery chemistry and biology data to guide preclinical drug design, optimization, and delivery strategies.
  • Engage, innovate, and collaborate with cross-functional colleagues and interdisciplinary teams
  • 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 support junior scientists and build relationships through coaching and mentorship with fellow scientists at all levels
  • Possess excellent written and verbal technical communication and the ability to constructively lead, guide 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 therapeutics
  • 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 Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

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

$184,500 - $321,200

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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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876