About this role
The Clinical Research Associate (CRA) is responsible for overseeing clinical trial sites to ensure compliance with regulations and quality standards. They build relationships with investigators, monitor study progress, and support site development and performance improvement. The role involves collaboration with cross-functional teams to facilitate trial operations.
Required Skills
- GCP
- ICH-GCP
- Site Management
- Clinical Trials
- Monitoring
- Data Management
- Study Coordination
- Regulatory Compliance
- CDMS
- eTMF
About MSD
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