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2 open listings
Roles posted by organizations here, alongside roles we found on employers’ own careers sites. Crawled roles say so on the card and send you to the employer to apply. Only show organizations on Career App
Moderna
Full-time
Lead sponsor-side oversight of nonclinical studies at Moderna's Canadian operations, managing GLP and non-GLP research from protocol development through final reporting. This role suits experienced study managers and monitors in the biopharmaceutical sector who can manage complex outsourced research programs, work with CROs, and drive regulatory compliance across a matrixed organization.
Listed on Moderna’s careers site · Apply there ↗
Gilead Sciences
United States - California - Foster City
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.
Listed on Gilead Sciences’s careers site · Apply there ↗