Senior Clinical Research Coordinator

Job Summary

Working remotely on a full-time basis, the Senior Clinical Research Coordinator will oversee day-to-day activities of clinical trials, ensuring compliance with Good Clinical Research Practice (GCP), managing protocol coordination, and maintaining regulatory documentation.

Key responsibilities

• Serves as the primary regulatory contact for assigned protocols and maintains regulatory binders/files
• Coordinates submissions to ancillary committees and communicates with the IRB and Sponsor regarding regulatory management
• Prepares and submits study amendments and regulatory files for auditing and monitoring visits

Required qualifications

• High School Diploma/GED with 5 years of clinical research experience, or
• 2 years of clinical research experience with a Bachelor's degree, or
• 1 year of clinical research experience with a Master's Degree