Remote Clinical Data Management Lead

Neurocrine Biosciences; California; Remote; USD 172,000 - 235,000; Full time

Benefits offered by this job

401(k) matching

Paid vacation

Health benefits

Remote work option

Job summary

Neurocrine Biosciences is seeking an Associate Director of Clinical Data Management to lead CDM activities across studies, ensuring high-quality, inspection-ready data. You will oversee data collection strategy, EDC builds, external data integration, and data reconciliation with cross-functional partners.

You will collaborate with Biostatistics, Programming, and Clinical Operations to ensure end-to-end traceability and timely delivery, while mentoring CDM staff and guiding modernization efforts

Qualifications

• BS/BA in computer science or life sciences with 10+ years in CDM.
• MS with 8+ years in clinical data management; PhD with 6+ years acceptable.
• Experience with SDTM standards and data integration.
• Strong vendor management and CRO oversight experience.

Responsibilities

• Provide operational leadership for CDM across studies to ensure inspection-ready data.
• Lead data collection strategy, EDC/database build, external data integration, and data delivery.
• Develop and execute CDM deliverables: DMPs, data review plans, SAS specs, edit checks.
• Collaborate with Biostatistics and Programming for end-to-end traceability.
• Oversee CROs/vendors; monitor performance, quality, and timelines.
• Represent CDM in study teams and vendor meetings; communicate risks and progress.
• Drive process improvements, standard libraries, and automation in CDM.

Skills

CDM leadership

Regulatory knowledge

SDTM mapping

Vendor management

Data standards

Cross-functional collaboration

Education

BS/BA in Computer Science or Life Science with 10+ years CDM

MS in CS/Life Science with 8+ years

PhD in relevant field with 6+ years

Tools

Medidata Rave

CDMS/EDC platforms

Job description

Neurocrine Biosciences is seeking an Associate Director of Clinical Data Management to lead CDM activities across studies, ensuring high-quality, inspection-ready data. You will oversee data collection strategy, EDC builds, external data integration, and data reconciliation with cross-functional partners.

You will collaborate with Biostatistics, Programming, and Clinical Operations to ensure end-to-end traceability and timely delivery, while mentoring CDM staff and guiding modernization efforts