Backed by GV.
About the role
We are seeking an experienced Associate Director or Director of Toxicology to join our nonclinical development team to support discovery and development programs, with a primary focus on nonclinical study oversight and toxicology. The primary focus of this role is to act as a key scientific and operational interface with external contract research organizations (CROs). Found on 1752vc Careers, the job board for startup and VC roles.
What they're looking for
- S., M.S., Ph.D., DVM, or advanced degree in Toxicology, Pharmacology, Veterinary Medicine, or a related biomedical science (or equivalent experience)
- 5–10 years of relevant experience in toxicology within pharmaceutical, biotech, or CRO settings
- Demonstrated experience writing and reviewing toxicology study plans/protocols and final study reports
- Direct experience managing or interfacing with CROs conducting in-life toxicology studies
- Experience serving as Study Monitor on GMP toxicology studies, including in-life visits, protocol/report review, and direct communication with CRO study directors
- Working knowledge of study budgets — able to review CRO quotes/change orders, track spend against budget, and flag scope or cost deviations to project teams
More about this role
We are seeking an experienced Associate Director or Director of Toxicology to join our nonclinical development team to support discovery and development programs, with a primary focus on nonclinical study oversight and toxicology. The primary focus of this role is to act as a key scientific and operational interface with external contract research organizations (CROs). The individual in this role will assume primary responsibility for the planning, execution, and monitoring of nonclinical studies, ensuring scientific rigor, data quality, and alignment with program timelines and regulatory expectations. This position requires strong scientific judgment, knowledge of regulatory guidance, effective communication, and the ability to independently manage multiple studies in a fast-paced, mission-driven environment. This role will also contribute to the preparation of nonclinical components of regulatory dossiers related documentation.
This individual will also serve as a scientific and strategic partner to cross-functional project teams, driving the design, execution, and interpretation of nonclinical toxicology studies in support of IND-enabling and lifecycle safety assessment...
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