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Clinical Research Associate Lead
1 week ago
About the Job: The Senior Clinical Research Associate (Sr. CRA) plays a critical role in the success of our clinical trials. We are seeking an experienced professional to lead our monitoring operations and provide guidance to junior staff members.
Your Key Responsibilities:
- Clinical Monitoring: Perform on-site monitoring activities, including review of patient recruitment, source data verification, and drug accountability.
- Site Management: Conduct qualification, initiation, monitoring, and termination visits of investigational sites.
- Documentation: Collect and maintain regulatory documentation, ensuring compliance with ICH GCP guidelines.
- Team Collaboration: Work closely with cross-functional teams to ensure successful project execution.
Requirements: A minimum of 4-5 years of clinical monitoring experience, including strong start-up experience, and a BA/BS or RN degree are required for this role.