Associate Manager, Clinical Data Management
Core
Managing clinical data management activities across the study lifecycle from startup to closeout, ensuring data quality and regulatory compliance for clinical trials.
Role type
Senior IC clinical data management manager
Builds
Clinical trial databases, data quality metrics, and regulatory documentation for pharmaceutical studies
Domain
Life sciences / Clinical research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
EDC build and specification creation, test script development, UAT execution, study document creation (DQMP, eCRF instructions, PDRP), eTMF management, data quality review facilitation, project timeline management, team mentorship
Preferred skills
Vendor coordination, post-production/migration planning, data health metrics reporting
Technologies
EDC systems, eTMF, Interactive eCRF, Safety Gateway
Responsibilities
Draft EDC build timelines and specifications; Create test scripts and execute UAT; Facilitate startup meetings and review meetings; Create and finalize study documents; Coordinate with clinical data managers and external vendors; Support data quality reviews and provide metrics; Plan and execute database lock activities; Mentor junior CDM staff
Seniority
Senior, hands-on IC with mentorship responsibilities
