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Adme Jobs (NOW HIRING)

We are seeking Associate Scientist-In Vitro ADME to join IQVIA Laboratories at Indiana. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If ...

Senior Advisor - Discovery ADME Project Leader

Boston, MA · On-site

$148.30K - $148.80K/yr

Senior Advisor -Discovery ADME Project Leader Organization Overview Lilly is a global healthcare leader headquartered in Indianapolis, Indiana. Our50,000employees around the world work to discover ...

We are seeking Associate Scientist-In Vitro ADME to join IQVIA Laboratories at Indiana. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If ...

Screening support to produce ADME in vitro data in support of driving discovery efforts within Pfizer WRD The position includes performing biological assays using automation technologies to generate ...

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Adme information

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$62K

$93.9K

$150K

How much do adme jobs pay per year?

As of May 30, 2026, the average yearly pay for adme in the United States is $93,868.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is an Adme job?

The role of an Adme (Absorption, Distribution, Metabolism, and Excretion) professional typically involves studying how drugs interact with biological systems. They analyze pharmacokinetics and pharmacodynamics to assess drug safety and efficacy. This job is crucial in pharmaceutical research and development, ensuring medications are effective and safe for human use. Adme scientists use laboratory techniques, computational models, and clinical data to predict drug behavior.

What are the key skills and qualifications needed to thrive in the Adme position, and why are they important?

To excel as an ADME (Absorption, Distribution, Metabolism, and Excretion) scientist, you typically need a strong background in pharmacology, biochemistry, or related life sciences, often supported by a relevant advanced degree. Familiarity with laboratory instrumentation, bioanalytical methods, and regulatory compliance frameworks such as GLP/GCP guidelines is essential. Attention to detail, strong analytical thinking, and effective teamwork skills help differentiate top candidates. These competencies are vital for generating high-quality data, ensuring regulatory compliance, and driving forward drug development processes.

What are some typical daily responsibilities of an ADME scientist?

ADME scientists spend their days designing and conducting experiments to assess how drugs are absorbed, distributed, metabolized, and excreted in biological systems. They analyze data using state-of-the-art lab equipment and software, prepare detailed reports and documentation, and present findings to project teams or regulatory agencies. Collaboration is common, as ADME scientists often work closely with chemists, toxicologists, and clinicians to interpret results and guide drug development strategies. Staying up to date with current regulatory requirements and scientific advancements is also a key part of the job.
What cities are hiring for Adme jobs? Cities with the most Adme job openings:
What states have the most Adme jobs? States with the most job openings for Adme jobs include:
Infographic showing various Adme job openings in the United States as of May 2026, with employment types broken down into 93% Full Time, and 7% Contract. Highlights an 93% In-person, and 7% Remote job distribution, with an average salary of $93,868 per year, or $45.1 per hour.
Discovery ADME Project Leader (Antibody Drug Conjugates, ADCs)

Discovery ADME Project Leader (Antibody Drug Conjugates, ADCs)

Lilly

Boston, MA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago


Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 62 frontline employees who took The Breakroom Quiz

11th of 70 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.

We are seeking an experienced, accomplished drug hunter as a Discovery ADME Project Leader focused on Antibody Drug Conjugates. The ideal candidate will provide deep mechanistic understanding of drug disposition, PK, and translational science, plus the ability to integrate biology, chemistry, and modeling. Experience with Bioconjugates Discovery and in project teams with antibody-drug conjugates (ADCs) and small format drug conjugates is advantageous. The successful candidate will bring exceptional scientific depth and acumen as an integral member of the project team to create bold Target Product Profiles, help establish design strategy and expectations, partner globally and cross-functionally and ensure teams are advancing The Right Molecule to The Right Study at The Right Time (our three R's). Geography for this position is open to Indianapolis IN, Louisville CO or Boston MA.

What You Will Do

  • Keep Safety as a priority.
  • Develop and implement integrated preclinical ADME strategies aligned with discovery stage, target product profile (TPP), design hypotheses being tested, and regulatory expectations.

As a Bioconjugates ADME Project Leader, bring integrated ADME subject matter expertise, driving comprehensive ADME strategy by aligning pharmacokinetics, metabolism, and mechanistic disposition data with early safety signals; interpret exposure-toxicity relationships, therapeutic index, and off-target liabilities to proactively de-risk programs and enable data-driven candidate selection decisions. Integrate ADME, pharmacology, and toxicology to enable translational simulations and modeling to support dose selection, design of PK/PD, efficacy and safety studies. Define stage-, modality-, and issue-appropriate screening, decision funnels (in silico, in vitro, in vivo to translational modeling). Guide compound design and optimization through data-driven design principles (clearance, permeability, solubility, DDI risk, transporter liabilities). Serve as the ADME strategy and science single-point-of-accountability on cross-functional program teams, translating ADME findings into actional design and test hypotheses. Collaborate closely with Medicinal Chemistry, DMPK, Toxicology, Pharmacology, and other Discovery Functions to drive high quality candidate selections. Contribute to go/no-go decisions using quantitative PK/PD, IVIVE, and mechanistic interpretation. Represent ADME in portfolio governance discussions and leadership reviews. Implement best practices, assay innovation, and automation where appropriate. Drive continuous improvement in data reporting, knowledge management, and decision frameworks. Seek and leverage AI and agentic tools where possible to pipeline data, interpret data and share results. Maintain inspection-ready documentation and alignment with regulatory expectations. Mentor, teach and grow junior scientists and contribute to functional capability building.

Basic Qualifications

  • PhD in Pharmaceutical Sciences, Pharmacokinetics, Pharmacometrics, Systems Pharmacology, Preclinical or Clinical Pharmacology, Drug Metabolism, Toxicology, Chemical Biology, or related field or Bachlors with 10+ years experince.
  • 6+ years of post-graduation industry experience in a drug discovery environment, driving discovery teams with understanding of the life cycle/flywheel (Design, Make, Test, Analyze) of a discovery project.

Additional Skill/Preferences

  • Deep subject matter ADME expertise, a working knowledge of medicinal chemistry and bioconjugates.
  • Exceptional written and verbal communication skills; ability to successfully navigate ambiguity and/or global cross-functional collaborations.
  • Demonstrated ability to translate complex technical concepts into strategic value for senior leadership and cross-functional partners.

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

$177,000 - $308,000

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