Associate Principal Scientist, Toxicology/Study Director
Merck · West Point, PA
Clinical OperationsFull-time$142k–$224kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Merck's Nonclinical Drug Safety department seeks an experienced toxicologist to serve as Study Director on GLP and non-GLP toxicity studies. The role involves directing in vivo studies, analyzing data from multiple disciplines, ensuring regulatory compliance, and collaborating across cross-functional teams from early discovery through late development.
What they're looking for
- Master's degree in toxicology, pharmacology, or related scientific discipline
- Minimum 8 years of relevant toxicology experience
- Minimum 5 years as Study Director in pharma, biotech, or CRO
- GLP Study Director experience with varied models and routes of administration
- Demonstrated understanding of FDA 21 CFR Part 58 (Good Laboratory Practices)
- Strong verbal and written communication skills
- Leadership ability and collaborative team orientation
What you'll be doing
- Serve as Study Director ensuring protocol compliance, regulatory adherence, and study execution across acute to chronic toxicology studies
- Critically analyze and interpret toxicology data from multiple disciplines and prepare findings for regulatory submissions
- Ensure regulatory rigor, identify risks proactively, and meet study timeline requirements
- Lead method development initiatives and participate in related scientific projects as needed
- Build collaborative relationships across technical, veterinary, and scientific teams
Privacy & handoff
This role links to Merck's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.