Clinical Research Assistant 251272

A Clinical Research Assistant supports clinical trials by conducting study visits, recruiting and screening participants, and managing data and samples. Key duties include scheduling, maintaining accurate records, ensuring adherence to protocols, and providing support to principal investigators and research coordinators.

Key Responsibilities

• Study Coordination: Schedule patient visits, manage study calendars, and assist with informed consent procedures.
• Patient Interaction: Screen, enroll, and educate participants while maintaining study compliance.
• Data Management: Enter accurate data into Case Report Forms (CRFs) and maintain study records.
• Sample Management: Collect, process, and ship biological samples as required.
• Safety Monitoring: Assist with collecting vital signs, conducting EKGs, and reporting adverse events.