ADME Biotransformation Scientist

Eli Lilly and Company • Indianapolis, IN

6d • $66,000 - $222,200

About The Position

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. ADME Biotransformation Scientist Company: Eli Lilly and Company Job Summary Eli Lilly and Company is seeking a highly motivated and skilled ADME Biotransformation Scientist to join our dynamic team. In this role, you will play a critical part in understanding the metabolic fate of novel therapeutic candidates, contributing directly to drug discovery and development programs.

Requirements

• Bachelor's degree with 6+ years of relevant industry experience
• Experience with LC-MS/MS and high-resolution mass spectrometry for metabolite identification and structural characterization.
• Experience in vitro ADME assays, including microsomal stability, hepatocyte metabolism, and reaction phenotyping.
• Experience with drug metabolism enzymes (e.g., CYPs, UGTs, FMOs) and their role in drug disposition.
• Experience designing experiments, troubleshooting technical issues, and interpret complex data independently.

Nice To Haves

• Master's degree with 3+ years of relevant industry experience
• Early career Ph.D. in Pharmaceutical Sciences, Pharmacology, Analytical Chemistry, Biochemistry, or a related scientific discipline with 0-3 years of post-doctoral or industry experience in ADME/DMPK, specifically focusing on biotransformation.
• Solid expertise in LC–MS/MS and high-resolution MS for metabolite identification
• Demonstrated hands-on experience in in vitro drug metabolism and biotransformation studies
• Excellent written and oral communication skills, with a proven ability to present scientific findings clearly and concisely.
• Strong collaborative spirit and ability to work effectively in a multidisciplinary team environment.
• Familiarity with regulatory guidelines related to drug metabolism and pharmacokinetics is a plus.
• Proven ability to work independently in a fast-paced research environment
• High standards for data quality, reproducibility, and scientific integrity.
• Interest in assay development, automation, or innovative analytical strategies
• Understanding pharmacokinetics, ADME and proficiency to communicate theory and concepts clearly
• Interest in data analysis and digital tools that enhance experimental biotransformation research
• Ability to balance multiple projects and handle competing responsibilities
• Collaborative team behaviors and aspiration to build and sustain relationships with R&D customers and the wider scientific community
• Exposure to modalities beyond small molecules would be considered a plus
• Experience in drug discovery and development
• Experience authoring regulatory and technical reports

Responsibilities

• Design, implement, and interpret in vitro and in vivo biotransformation studies to elucidate metabolic pathways, identify metabolites, and determine mechanisms of drug metabolism.
• Apply and develop innovative analytical techniques, including LC-MS/MS and high-resolution mass spectrometry, for metabolite identification, quantification, and structural elucidation.
• Conduct experiments to assess drug-drug interaction potential, including reaction phenotyping and enzyme induction/inhibition studies.
• Collaborate cross-functionally with medicinal chemists, pharmacologists, toxicologists, and other ADME scientists to integrate biotransformation data into drug discovery and development strategies.
• Prepare detailed scientific reports, presentations, and contribute to regulatory submissions.
• Evaluate and implement new technologies and methodologies to enhance biotransformation capabilities.
• Mentor junior scientists and contribute to a culture of scientific excellence and continuous learning.
• Maintain accurate and thorough laboratory records and ensure compliance with all safety and regulatory guidelines.

Benefits

• 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).

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level