Jobs at Neurocrine Biosciences

Sr. Analyst responsible for executing daily quality control checks on commercial life sciences datasets (specialty pharmacy, IQVIA, CRM) and performing root cause analysis on data anomalies.…See more Will support data ingestion and transformation validation in Databricks, maintain data dictionaries and quality rule libraries, and collaborate across business and technical teams to ensure data governance compliance. The role requires proficiency in SQL and hands-on Databricks experience, with opportunity to research and implement emerging data quality tools like Monte Carlo to improve efficiency and scalability.

Lead enterprise AI platform strategy and execution at a biotech company, driving end-to-end program delivery across engineering, data, cybersecurity, and product teams. Own platform health, KPIs, and telemetry; establish governance, safety guardrails, and regulatory compliance for AI-enabled solutions in a regulated environment.…See more Define multi-year AI roadmaps, coordinate cross-functional dependencies, and orchestrate Agile delivery while partnering with legal, compliance, and tech enablement to ensure scalability, security, and enterprise adoption.

A Program Manager for Technical Operations at a bioscience company supporting CMC (Chemistry, Manufacturing, and Controls) and pharmaceutical development activities. The role manages complex, cross-functional programs across Drug Substance/API Development, Analytical Development, Drug Product development, Manufacturing, Supply Chain, and Quality disciplines throughout the product lifecycle.…See more Responsibilities include risk mitigation, decision documentation, process improvement, stakeholder alignment, and integration of technical plans and dependencies across multiple teams and workstreams. Requires 6+ years of program/project management experience (or equivalent with advanced degree) with direct CMC or Technical Operations support in a pharmaceutical or biotech environment.

Sr. Specialist overseeing quality assurance systems, records management, and compliance in a pharmaceutical/biotech GxP-regulated environment.…See more Responsibilities include managing electronic quality systems, processing controlled documents and SOPs, supporting inspections and audits, analyzing quality metrics and dashboards, leading process improvement initiatives, and mentoring junior staff. Requires a bachelor's degree with 4+ years of pharma/biotech QA experience (or master's with 2+), strong knowledge of FDA/ICH/GMP/GLP/GCP regulations, proficiency with QMS and LMS platforms, and demonstrated leadership and analytical capabilities.

Senior IT Program Manager supporting the execution of moderately complex IT initiatives within a pharmaceutical company's Value Management Office. Leads or supports cross-functional technology projects from initiation through stabilization, with responsibility for scope, schedule, budget, quality, compliance, and business outcomes.…See more Requires 4+ years of IT experience in a pharma/biotech environment with FDA regulation exposure and hands-on knowledge of validated applications, web technologies, databases, and Microsoft application stack (SQL Server, Oracle, Java, web standards).

Lead commercial data management for a biotech company, overseeing data quality, validation, and governance processes across field and internal reports, analytics systems, and business operations. Design and implement data governance policies, standards, and best practices while managing cross-functional projects in a matrixed environment.…See more Requires 6+ years in pharmaceutical/biotech commercial operations or data management, expert knowledge of commercial biopharma data ecosystems, and proficiency with tools including Excel, Power BI, Tableau, Databricks, SQL, and Python. Ensure compliance with HIPAA and regulatory requirements while mentoring junior team members and communicating data insights to technical and business stakeholders.

Lead commercial data management activities for a biotech company, overseeing data quality-control processes, validation workflows, and governance policies. Collaborate with cross-functional stakeholders to ensure data accuracy across field reports, analytics, and business systems while identifying process improvements.…See more Manage documentation, mentor junior team members, and translate complex data concepts for both technical and business audiences. Requires 6+ years in pharmaceutical/biotech commercial operations or data management, expertise with tools like SQL, Python, Power BI, Tableau, and Databricks, and deep familiarity with commercial biopharma data sources and HIPAA compliance.

Principal Specialist overseeing clinical data management for pharmaceutical studies, responsible for database lock coordination, CRO performance monitoring, and ensuring quality control and audit procedures meet departmental standards. The role requires running data review listings, coding medical history and adverse event data using MedDRA, coding concomitant medications using WHO Drug dictionaries, and collaborating with database programmers to ensure CDISC/SDTM compliance.…See more Requires 8+ years of pharma industry experience (or equivalent with advanced degree), strong knowledge of Good Clinical Data Management Practices, and demonstrated ability to lead and manage teams across multiple projects.

Sr. Principal Specialist will oversee clinical database programming operations, including review/cleaning programs, validation procedures, database migrations, SAS dataset creation, and vendor management within a pharmaceutical environment.…See more The role requires hands-on technical expertise in Medidata Rave, SAS, and SQL alongside strategic leadership of cross-functional teams and oversight of regulatory compliance, inspection readiness, and system implementations. Responsibilities include proactive risk mitigation, evaluation and adoption of new technologies, and acting as a technical liaison across Clinical Data Management, Clinical Operations, Regulatory, and IT. The ideal candidate combines 8+ years of clinical database programming experience (or equivalent with advanced degree) with expert knowledge of CDISC standards, GCP regulations, and end-to-end drug development processes.

Senior Systems Engineer responsible for planning and implementing security patches across enterprise Linux and Windows server environments in AWS, Azure, and hybrid infrastructure. Design and operate automation platforms (AWS Systems Manager, Ansible, SCCM/Intune) to scale vulnerability management and remediation across cloud and on-premises fleets.…See more Partner with security, infrastructure, network, and compliance teams on patch testing, deployment sequencing, rollback procedures, and audit-ready documentation in a regulated (GxP/SOX/21 CFR Part 11) environment.

Lead clinical data management strategy, governance, and operations across a portfolio of clinical development programs in a biopharmaceutical environment. Manage CDM leaders and professionals, oversee data integrity initiatives, regulatory compliance, and vendor relationships while driving process improvements and technology modernization.…See more Requires 10–14+ years of clinical data management experience in pharma/biotech/CRO settings, with deep expertise in EDC platforms (Medidata Rave preferred), clinical data standards (CDASH, SDTM), GCP, ICH guidelines, and proven senior leadership capability.