Clinical Data Management Associate
Job Summary
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 activities
Required qualifications
- Undergraduate 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
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