Contract Clinical Research Associate

Job Summary

A company is looking for a Clinical Research Associate (Contractor).

Key Responsibilities

• Ensure compliance with clinical trial protocols and regulatory obligations during site monitoring
• Conduct on-site and remote monitoring activities, including source document verification
• Prepare and submit reports on investigational site findings and maintain tracking systems

Required Qualifications

• Minimum Bachelor's degree in a life science-related field, RN certification, or equivalent
• 3+ years of experience in a clinical trials research environment, specifically in vitro diagnostics
• General knowledge of regulatory requirements and Good Clinical Practice (GCP)
• High proficiency in Veeva Vault and Medrio
• Strong organizational skills and attention to detail