Senior Clinical Research Associate

Job Summary

To support clinical monitoring efforts, the full-time Senior Clinical Research Associate will manage site activities, ensure compliance with protocols, and collaborate with cross-functional teams in a remote or office setting.

Key responsibilities

• Manage site initiation, monitoring, and close-out activities for clinical trials
• Ensure compliance with regulatory requirements and study protocols
• Collaborate with project teams to address site-related issues and enhance study performance

Required qualifications

• Bachelor's degree in a related field or equivalent experience
• At least 3 years of experience in clinical research monitoring
• Strong understanding of Good Clinical Practice (GCP) guidelines
• Experience with electronic data capture (EDC) systems
• Ability to travel as needed for site visits