Listed on Gilead Sciences’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This VP-level role leads Gilead's nonclinical safety and pathobiology group, overseeing toxicology, pathology, and environmental assessments that support drug candidates from research through regulatory approval. The position suits a seasoned pharmaceutical scientist with 20+ years of experience and recognized expertise in nonclinical drug development who can manage a team of PhD-level specialists and navigate complex global regulatory requirements.
Our summary, not Gilead Sciences’s wording. The full posting is on their site.
What they ask for
Required
- PhD in pharmacology, toxicology, pathology or related discipline
- At least 20 years of pharmaceutical or CRO research/development experience
- Knowledge of global regulatory guidelines for nonclinical safety studies
- Leadership and management of PhD-level scientists
- Cross-functional collaboration across global stakeholders
Nice to have
- DABT certification
- DACVP certification
- ERT certification