Head of Clinical Data Management
Neurocrine BiosciencesAbout the role
Who We Are:
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:
Provides strategic and operational leadership for clinical data management activities across multiple clinical programs to deliver high-quality, inspection-ready clinical data supporting clinical development, regulatory submissions, and business decision-making. May function as the lead for Clinical Data Management or as a senior leader within the function based on organizational needs.Accountable for overall Clinical Data Management strategy, operating model, budget and resource planning, vendor ecosystem, and development of leadership capability within the function when serving in a functional leadership capacity.
Ensures execution quality across the clinical data lifecycle, including data collection strategy, EDC/database build, external data integration, data review, reconciliation, database lock readiness, and vendor oversight. Establishes data quality plans, operational metrics, and risk-based approaches to improve predictability, reduce rework, and ensure timely delivery of reliable clinical data.
Collaborates cross-functionally to enable fit-for-purpose data collection, cross-study consistency, and end-to-end traceability from protocol and CRF design through analysis-ready datasets. Leads continuous improvement and technology enablement initiatives, including scalable EDC build methodologies, standard libraries, automation, AI-enabled data review workflows, and solutions supporting end-to-end biometrics standardization.
Manages and develops internal staff and external partners, strengthening leadership capability within the function while ensuring effective resource planning, vendor governance, and succession planning.
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Your Contributions (include, but are not limited to):
Direct clinical data management activities across assigned studies, programs, and/or
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