Scientist, Safety
Neurocrine Biosciences
August 22, 2026
Full-time
Remote friendly (San Diego, CA)
Worldwide
Clinical Research and Development
Role: Pharmacovigilance Scientist supporting safety surveillance and risk management for Neurocrine's neurological, psychiatric, endocrine, and immunological products throughout their lifecycle. Responsibilities: participate in safety signal detection and investigation, execute risk management plans across development and post-approval, review safety data, prepare safety input for regulatory submissions, and support safety-related documentation and audits. Collaborate with multidisciplinary teams across R&D, regulatory, and clinical functions. Requirements: BS/BA in a scientific field or RN with 2+ years in pharmacovigilance or clinical research; or MS/MA, PharmD, or PA with relevant experience. Key skills include knowledge of ICH, US/EU pharmacovigilance regulations, safety systems (ARISg, Argus), and signal evaluation, with strong analytical, communication, and teamwork abilities. Preferred: experience with aggregate safety data and regulatory reporting. High-Value: focus on safety surveillance for neurological and psychiatric indications, lifecycle safety management, and compliance with global pharmacovigilance standards. Work setup: unspecified, with a salary range of $89,800-$123,000, plus bonus, equity, and benefits.