Senior Scientist, Non-Regulated Bioanalysis and PK Operations

Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit  neurocrine.com , and follow the company on  LinkedIn ,  X , Facebook and YouTube . ( *in collaboration with AbbVie ) About the Role: The Senior Scientist, Bioanalysis & PK Operations will support the planning, coordination, and execution of non-regulated bioanalytical, PK, and TK activities. The role will manage BA/PK/TK study outsourcing, CRO and vendor relationships, critical reagent outsourcing, sample and shipping logistics, contracting and invoicing, study tracking and documentation, and cross-functional operational workflows. The position will partner closely with Bioanalysis, PK, in vivo, and project teams to ensure efficient study execution and timely delivery of high-quality data. _ Your Contributions (include, but are not limited to): Coordinate non-regulated Bioanalysis and PK operations from study request through completion, including study tracking, documentation, and data management workflows Coordinate and manage outsourcing of BA, PK, and TK studies, including CRO selection/engagement, study setup, monitoring, timelines, deliverables, and issue resolution Manage outsourcing and logistics for critical reagent development and production, including vendor coordination, shipping, tracking, and inventory Support PK study design, planning, execution, and monitoring in collaboration with PK, BA, in vivo, and project teams Manage domestic and international sample and reagent shipments, including applicable shipping requirements and documentation Support CRO/vendor management, contracting, purchase orders, invoicing, and study/reagent logistics for non-regulated activities Coordinate sample and study data management, from physical sample assets through digital databases, study documentation, and data delivery Serve as an operational representative on discovery and development project teams, supporting study readiness, cross-functional alignment, and timely execution Contribute to the preparation and review of study reports and IND/CTA-enabling documentation, as appropriate Requirements: PhD in pharmaceutical sciences, pharmacokinetics, bioanalysis, analytical chemistry, biology, or related discipline with 2+ years of relevant experience; OR MS with 4+ years; OR BS with 6+ years of relevant industry experience Experience supporting nonclinical PK, pharmacology, toxicology and/or bioanalytical studies in a pharmaceutical/biotechnology or CRO environment Experience with CRO/vendor management and outsourcing, including study coordination, timelines, deliverables, contracting, and invoicing Working knowledge of bioanalysis and PK study workflows, including sample management, study documentation, and data/reporting processes Experience coordinating biological sample and/or critical reagent shipments, including domestic and international logistics Strong project management, organizational, communication, and cross-functional collaboration skills with the ability to manage multiple