Senior Clinical Research Associate

Job Summary

To support clinical trials, the full-time Senior Clinical Research Associate will manage site monitoring activities, ensuring compliance with protocols and regulatory requirements, while working remotely or onsite across multiple US locations.

Key responsibilities

• Oversee site selection, initiation, monitoring, and closeout activities for clinical trials
• Ensure adherence to study protocols, regulatory guidelines, and Good Clinical Practice (GCP)
• Collaborate with cross-functional teams to facilitate effective communication and project progress

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 clinical trial processes and regulatory requirements
• Experience with electronic data capture (EDC) systems
• Ability to travel as needed for site visits