Director, Standards & Integrations

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 , and follow the company on Linked In, X, Facebook and You Tube. (
* in collaboration with Abb Vie)

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 , and follow the company on Linked In, X, Facebook and You Tube. (
* in collaboration with Abb Vie)

About The Role

The role will lead the execution of the Standards and Integration strategy through automation-centric, AI-enabled biometrics workflows that scale and accelerate delivery across the clinical development portfolio, from protocol finalization through final Tables, Figures, and Listings (TFLs). Grounded in reusable metadata, lifecycle governance, content reuse and responsible-AI controls, this role ensures regulatory-compliant data collection, analysis, and reporting and sustained inspection readiness.

The Director partners closely with Data Management, Statistical Programming, Biostatistics, Data Science, IT and Quality to operationalize data and analysis requirements into integrated workflows and to design tools that enable seamless handoffs across functions. Reporting to the Executive Director, the role leads a team of standards and automation professionals, including subordinate leaders, manages strategic outsourcing and external vendors, and maintains external connections to stay current with, and helps shape, industry standards.

Your Contributions (include, But Are Not Limited To)

• Translate the Standards and Integration strategy into operational priorities, execution plans and measurable outcomes aligned with company goals and ADS leadership; lead, coach and develop the team, including subordinate leaders
• Lead 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 aligned to CDISC expectations, with strong linkage between CDASH-compliant data collection, downstream CDISC-compliant SDTM/ADaM data, and Neurocrine standard analysis and reporting
• Submission readiness:
  Oversee design and quality of submission-critical outputs, including the Define-XML package, ensuring traceability, consistency and an inspection-readiness mindset
• Lead the design, development, validation and deployment of low/no-code and programmatic (SAS, R, Python, SQL) automations, including reusable macros and functions, ETL workflows, and data quality checks and alerts, which improve:
  • Standards adherence and…