Strong experience in Clinical Data Management within the pharmaceutical, biotechnology, CRO, or clinical research industry.
Demonstrated experience managing complex clinical studies, programs, or multiple data management workstreams.
Strong knowledge of clinical data management processes and clinical trial operations.
Working knowledge of CDISC standards, particularly SDTM.
Experience coordinating global and cross-functional teams.
Experience with project planning, milestone management, risk assessment, and deliverable tracking.
Exposure to Health Authority submissions and regulatory documentation.