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Supporting the delivery and oversight of clinical and patient-reported data, the full-time Associate / Senior Associate, Clinical Data Management will manage and review clinical data within EDC platforms, collaborating with cross-functional teams from study startup through closeout in a remote environment.
Key responsibilities: Manage and review clinical and ePRO data, including video-based data collection Develop Data Management Plans, CRF Specifications, eCRFs, and study documentation Support data transfers, exports, migrations, and reconciliation activitiesRequired qualificationsUndergraduate degree or equivalent professional experience Experience supporting clinical study protocols and data management activities Professional experience within biopharma, pharmaceutical, CRO, or clinical site environments Knowledge of GCP, ICH, HIPAA, GDPR, and FDA requirements Experience with clinical research technologies and health data collection systems

Also on the board Same function, level within a rung

Level

Lead

Location

New York, NY

Occupation

Clinical Data Managers

Industry

Research and Development in Biotechnology

Posted

2 days ago

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