Associate Director Toxicology
$155,000–$193,200 year
Hybrid · Princeton, New Jersey, United States or San Diego, California, United States
Job Summary
The Associate Director of Toxicology will oversee Translational Science preclinical safety assessment/toxicology deliverables, contributing to the development of products and programs in support of the pipeline. Responsibilities include planning experimental safety assessment/toxicology programs, managing CROs for quality and compliance, and reviewing toxicology reports. The ideal candidate will possess knowledge in preclinical study types, GLP, ICH and FDA guidance, and have extensive experience in cross-functional project collaborations. Strong communication and problem-solving skills, along with the ability to work independently and with various stakeholders, are essential.
Required Qualifications
- BS or MS in a relevant discipline or a related field
- 8 years of relevant experience in pre-clinical safety assessment/toxicology supporting drug development
Desired Qualifications
- DABT Certification strongly preferred
- Understanding of drug development process and principles of preclinical safety assessment/toxicology
- Experience working in cross-functional project teams
- Study monitoring experience on Good Laboratory Practices (GLP) safety assessment/toxicology studies at CROs
- Demonstrated skills in influencing, facilitation, development, and problem solving
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.