Associate Director, Study Toxicologist
$178,000–$218,000 year
On-siteConshohocken, Pennsylvania, United States
Job Summary
Support the design and execution of nonclinical studies, including toxicology, PK, ADME, and bioanalytical work, while providing scientific oversight of outsourced programs. Manage vendor interactions, study startups, and timeline tracking to ensure data accuracy and alignment with regulatory submissions. Review protocols, monitor study conduct at CROs, and interpret final reports for completeness and scientific rigor. Partner with Nonclinical Development leads to contribute to integrated development plans and nonclinical strategy. This role is part of the Nonclinical Development team within Research, supporting Madrigal's MASH portfolio and Rezdiffra development.
Required Qualifications
- PhD (or equivalent) in Toxicology, Pharmacology, DMPK, or a related scientific discipline
- Relevant pharmaceutical or biotechnology industry experience supporting nonclinical development programs
- 10+ years of relevant experience
- Experience managing outsourced nonclinical studies with CROs, including protocol and report review
- Strong attention to detail
- Ability to manage multiple studies simultaneously
- Excellent written and verbal communication skills
Desired Qualifications
- Experience with small molecule and/or siRNA programs
- Experience supporting late-stage nonclinical studies, including reproductive and developmental toxicology (DART) and carcinogenicity studies
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