Associate Data Manager
Core
Ensure quality, accuracy, and integrity of clinical trial data throughout the study lifecycle by performing quality control, investigating discrepancies, and supporting data review and reconciliation.
Role type
Associate Data Manager (Clinical Trials)
Builds
Clinical trial data deliverables and audit-ready documentation
Domain
Life Sciences / Clinical Research / eClinical
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Data quality control, discrepancy investigation, study documentation management, schedule coordination, data metrics tracking, CAPA support, regulatory compliance knowledge, analytical problem-solving
Preferred skills
Pharmaceutical/biotech industry experience, GCP/FDA/EMA regulatory knowledge, eClinical technology exposure (eCOA, ePRO, RTSM), SQL/SAS proficiency, CDISC standards knowledge
Technologies
eCOA, ePRO, eConsent, RTSM, IRT, SAS, SQL, CDISC (SDTM)
Responsibilities
Perform quality control and consistency checks on study data outputs; Investigate data discrepancies and collaborate with scientific teams to resolve issues; Support creation and review of Data Management Plans and Data Transfer Specifications; Coordinate updates to Clinical Data Management task schedules; Assist with data management metrics and study tracking; Serve as primary point of contact for client reconciliation feedback; Maintain high-quality documentation and audit-ready records.
Seniority
Junior to Mid-level, hands-on IC
