Neurocrine Biosciences is a leading biopharmaceutical company dedicated to discovering, developing, and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine, and immunological disorders. This role involves performing day-to-day activities related to Toxicology and Safety Pharmacology study contracts. The specialist will work with contract Research Organizations (CROs) to place studies supporting the company’s development compounds, coordinate study archiving, manage Test Article (TA) shipments, and review/approve invoices. The position requires proficiency in Neurocine Agiloft Portal and Coupa systems, and periodic review of study tracking databases for accuracy. The role also involves staying updated with current regulatory guidelines.
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Job Type
Full-time
Career Level
Mid Level