Principal Data Engineer, Biometrics

Who We Are:

About the Role:

This role will serve as an experienced data engineering professional responsible for designing, developing, implementing, and maintaining complex data engineering solutions that support Neurocrine's Clinical programs, including Clinical Data Management, Statistical Programming, and Biostatistics functions. This role sits on the regulated data path that runs from clinical data collection through analysis datasets, and ultimately submission to regulatory agencies. The ideal candidate brings fluency in CDISC standards (CDASH, SDTM, ADaM, and controlled terminology) and other industry-standard clinical data models, along with the software engineering discipline needed to build, validate, and maintain tools in a GxP environment. Work directly targets faster study database builds, higher data quality, more efficient dataset and output generation, and the ability of Biometrics to scale as Neurocrine's pipeline grows.
This role analyzes and resolves complex technical challenges, partnering across functions to evaluate underlying needs, recommend appropriate solutions, and implement scalable improvements. The position requires sound judgment and the ability to translate business requirements into effective, sustainable data engineering solutions.
The role contributes to the development and implementation of technical standards and best practices, supports the adoption of solutions, and ensures appropriate documentation, training, and ongoing support to sustain long-term effectiveness.

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Your Contributions (include, but are not limited to):

• Collaborate cross-functionally with clinical Data Management, Statistical Programming, and Biostatistics to evaluate complex workflows, identify opportunities for improvement, define solution requirements, and identify measurable success criteria for data engineering initiatives
• Translate Biometrics processes into maintained, production-grade data products with clear ownership, versioning, and support
• Design, build, and maintain pipelines that move clinical data from collection systems (EDC, eCOA, central labs, and other vendors) into standards-compliant, analysis-ready datasets
• Develop automation across the CDISC data flow, including CDASH-aligned collection, SDTM dataset generation, and support for ADaM and TFL production, maintaining traceability end to end
• Build data quality and review tools, such as automated checks and outlier detection, that shift review from manual inspection to exception-based workflows
• Develop tools that accelerate study start-up, including protocol-to-SoA-to-CRF review, standards-based EDC database build, and protocol-to-SAP and SAP-to-TFL shell automation
• Support Medical Writing and Biostatistics with automated, standards-driven document outputs
• Assist in defining vendor data transfer specifications and implementing direct vendor-to-EDC and vendor-to-lake transfers in partnership with integration and platform colleagues
• Apply established SDLC and computer system validation practices for GxP-related systems, including requirements, risk assessment, testing, traceability, change control, and release documentation, to ensure compliant, inspection-ready solutions
• Support successful implementation and adoption of delivered tools through user training, documentation, and ongoing feedback, and measure impact through usage, time saved, and quality improvements
• Collaborate with platform and AI engineering colleagues so Biometrics data products align with the enterprise data lake, governance model, and downstream analytics
• Serve as a technical resource and advisor to Biometrics and Clinical stakeholders, providing technical recommendations, evaluating emerging technologies and vendor solutions, and recommending solutions that address business and technical requirements
• Other job-related duties as assigned

Requirements:

• Bachelor's Degree in Computer Science, Engineering, Bioinformatics, Statistics, or a related field AND 6+ years in data engineering, statistical programming, or clinical data management, including work in a regulated clinical environment OR
• Master's Degree in Computer Science, Engineering, Bioinformatics, Statistics, or a related field AND 4+ years as noted above
• Advanced knowledge in CDISC standards, including CDASH, SDTM, ADaM, controlled terminology, and define.xml, with an understanding of their application across clinical data collection, analysis, and regulatory submission
• Demonstrated experience designing, developing, and maintaining complex, production-grade data engineering solutions supporting clinical data management, statistical programming, or biostatistics
• Strong proficiency in Python, SQL, database design, and data modeling, with working knowledge of SAS and/or R
• Advanced knowledge of software engineering best practices, including Git/GitHub, CI/CD, automated testing, and maintainable code development
• Experience with clinical data structures and integration across EDC, eCOA, CTMS, and external vendor systems
• Experience with cloud computing platforms, preferably AWS; familiarity with Databricks and/or Spark is a plus
• Experience applying GxP software validation (CSV/CSA), 21 CFR Part 11 requirements, and risk-based validation practices to regulated software solutions
• Strong understanding of FDA clinical study data submission expectations, including the Study Data Technical Conformance Guide and conformance tools such as Pinnacle 21
• Experience operationalizing AI/LLM workflows, including prompt and retrieval design, output evaluation, monitoring, and validation appropriate for regulated environments
• Working knowledge of statistical concepts and methods, including descriptive statistics, probability, and hypothesis testing

• Experience in the biopharmaceutical industry or a contract research organization (CRO) supporting clinical trials
• Demonstrated ability to analyze and resolve complex technical and business problems, applying sound judgment to develop innovative and effective solutions
• Strong analytical, critical thinking, and problem-solving skills, with the ability to evaluate alternative solutions and consider cross-functional impacts
• Excellent communication, collaboration, and influencing skills, with demonstrated ability to collaborate effectively with cross-functional stakeholders to support alignment and adoption of solutions
• Demonstrated ability to provide technical guidance, contribute to best practices, and support the development of less-experienced colleagues without direct supervisory authority
• Strong organizational and prioritization skills, with the ability to lead complex projects and initiatives, managing competing priorities and delivering results aligned with functional objectives
• Ability to identify opportunities for continuous improvement, recommend and implement process improvements and scalable solutions that enhance operational effectiveness

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Neurocrine Biosciences is an EEO/Disability/Vets employer.

We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don’t line up to exactly what we have outlined in the job description.

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The annual base salary we reasonably expect to pay is $132,700.00-$182,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.