Global Head of Clinical Data Management & Data Quality

AbCellera Biologics Inc.; United States; A distancia; USD 180.000 - 280.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Equity

Annual performance bonus

6% 401K

Active Lifestyle Allowance $1,500

Comprehensive health benefits

Professional development

Descripción de la vacante

AbCellera Biologics Inc. is seeking an experienced Senior Director of Clinical Data Management to define and execute a global data strategy.

You will build a high-performing team, safeguard data integrity, and ensure inspection readiness across development programs in multiple therapeutic areas. You will lead end-to-end data management, oversee eCRF builds, data cleaning, and database locks, while partnering with Clinical Development, Quality, and Biostatistics to uphold stringent regulatory

Formación

• Advanced degree with 10+ years in industry and 5+ years in people management.
• Proven experience building and leading clinical data management teams.
• End-to-end data management for clinical trials including DM deliverables.

Responsabilidades

• Lead global clinical data management strategy and team growth.
• Ensure data quality, regulatory readiness, and audit support across trials.
• Oversee CRO/vendor governance and budget oversight.
• Collaborate with Clinical Development, Quality, Biostatistics, and Regulatory.
• Drive data standards, eCRF design, data cleaning, and database locks.

Conocimientos

Strategic leadership

Team development

Regulatory compliance

Cross-functional collaboration

Vendor management

Audits & inspection readiness

CDISC standards (CDASH/SDTM)

Data integrity & quality

Educación

Master's degree in Life Sciences/Statistics/Data Science

Herramientas

Medidata Rave

EDC platforms

Define-XML/SDTM tooling

Descripción del empleo

AbCellera Biologics Inc. is seeking an experienced Senior Director of Clinical Data Management to define and execute a global data strategy.

You will build a high-performing team, safeguard data integrity, and ensure inspection readiness across development programs in multiple therapeutic areas. You will lead end-to-end data management, oversee eCRF builds, data cleaning, and database locks, while partnering with Clinical Development, Quality, and Biostatistics to uphold stringent regulatory