Associate Director Biometrics Standards & Integrations
AI summary of the role
This role leads the strategy to scale and accelerate biometrics deliverables by implementing automation-centric, AI-enabled workflows within a regulatory compliant framework.
No longer in the current catalog. Last included 2026-09-09. Check the employer’s posting for availability.
What you’ll do
- Implement and champion continuous improvement of foundational standards that enable automation across studies (rulesets, mappings, reusable templates, controlled specifications).
- Drive standards implementation aligned to CDISC expectations, linking CDASH-compliant data collection to downstream CDISC-compliant analysis/reporting.
- Build and deploy low/no-code automations to improve standards adherence, handoff quality, repeatability, and inspection readiness.
- Enable governed AI use within Biometrics, including use cases, access restrictions, peer review, and automated checks.
What you’ll bring
- BS/BA + 10+ years, MS + 8+ years, or PhD + 5+ years of relevant biotech/pharma/CRO clinical development experience.
- Deep knowledge of CDASH and CDISC industry standards (SDTM, ADaM, Define.xml) and regulatory requirements.
- Advanced SAS or R proficiency; Python and SQL strongly preferred.
- Experience with Medidata Rave EDC build and content reuse (CRF standards, edit checks, libraries).
Technologies
CDASH · CDISC · SDTM · ADaM · Define-XML · SAS · R · Python · SQL · Medidata Rave EDC · GxP
About Neurocrine Biosciences
Discovers, develops, and commercializes drugs for under-served neurological, neuroendocrine, and neuropsychiatric disorders; lead product INGREZZA treats tardive dyskinesia and Huntington's chorea.
Public · 2000–5000 people
Source and classification
Internal deployment & tooling · Evidence for this classification:
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 neurocrine.com, and follow the company on LinkedIn, X and Facebook. (*in collaboration with AbbVie) About the Role: 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
More from the job description
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. What We Do: 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 neurocrine.com, and follow the company on LinkedIn, X and Facebook. (*in collaboration with Abb [... source excerpt omitted ...] ion, 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. _ Your Contribut [... source excerpt omitted ...] ools, technologies, and methodologies to enhance efficiency and effectiveness, while fostering collaboration with peers across relevant functional areas Other duties as assigned Requirements: BS/BA degree AND 10+ years of relevant biotech/pharma/CRO clinical development experience OR Master’s degree AND 8+ years of related biotech/pharma/CRO clinical development experience OR PhD AND 5+ years of related biotech/pharma/CRO clinical development experience Considered an expert within the company and may have external presence in area of expertise Applies in-depth knowledge of own function, business / commercial / scientific expertise to solve critical issues successfully and in
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