Clinical Research Associate (Los Angeles Based)
ProPharma(18 days ago)
About this role
ProPharma is seeking a Contract Clinical Research Associate to manage and support clinical study projects, primarily focusing on site management and monitoring activities. The role involves ensuring regulatory compliance, maintaining communication with study sites, and supporting the overall clinical trial process.
Required Skills
- GCP
- ICH
- Pharmacovigilance
- Clinical Monitoring
- Regulatory Compliance
- Data Management
- Site Management
- EDC
- Source Data Verification
- Clinical Trials
About ProPharma
propharmagroup.comProPharma helps navigate the complexities of drug development and ensure patient health and safety throughout the product lifecycle.
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