Associate Director Biometrics Standards & Integrations

Who We Are:

At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs.

Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine, and neuropsychiatric disorders. The company’s diverse portfolio includes FDA‑approved treatments for tardive dyskinesia, chorea associated with Huntington’s disease, classic congenital adrenal hyperplasia, 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 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 , and follow the company on Linked In, X and Facebook. (
* in collaboration with Abb Vie)

Responsible to execute on strategy to scale and accelerate biometrics deliverables by leveraging existing standards and processes to implement automation‑centric, AI‑enabled workflows that result in regulatory compliant data collection, analysis, and reporting. This role works closely with project leads in Data Management, Statistical Programming and Biostatistics to operationalize existing data and analysis requirements into automation‑centric, AI‑enabled workflows in a regulatory compliant framework deeply rooted in reusable metadata, lifecycle governance, content reuse and responsible‑AI controls.

This role will identify opportunities and partner with leadership to prioritize and design tools that facilitate seamless integration among Data Management, Statistical Programming and Biostatistics to scale and support a growing portfolio and ensure regulatory compliance and inspection readiness.

• Implement and champion continuous improvement of foundational standards that enable automation and consistent execution across studies (e.g., standards rulesets, mappings, reusable templates, workflow checklists, and controlled specifications)
• Drive standards implementation and operationalization aligned to CDISC expectations, including strong a linkage between CDASH‑compliant data collection and downstream CDISC‑compliant data and subsequent Neurocrine standard analysis/reporting
• Support design and quality of submission‑critical outputs, including the Define‑XML package, ensuring traceability, consistency and an inspection‑readiness mindset
• Build and deploy low/no‑code automations that improve: standards adherence and consistency, handoff quality between Data Management, Statistical Programming and Biostatistics, repeatability of analysis and reporting workflows, inspection readiness through controlled outputs and documentation
• Enable governed AI use within Biometrics (creating and implementing use cases, access restrictions, peer review, and automated checks)
• Define inspection‑ready evidence for automated/AI‑assisted outputs
• Provide training and technical support to end users for effective adoption and utilization of AI and automation solutions
• Shape, with buy‑in and endorsement from ADS Leaders, the ADS technology strategy by guiding the adoption of innovative technologies and encouraging a culture of creativity and continuous improvement
• Drive innovation within biometrics by identifying and implementing new tools, technologies, and methodologies to enhance efficiency and effectiveness, while fostering collaboration with peers across relevant functional areas
• Other duties as assigned

• BS/BA degree AND 10+ years of relevant biotech/pharma/CRO clinical development…