Job Summary:
The CRPM is responsible for coordinating and administering clinical trials under the direction of a principal investigator. This role involves participant recruitment, data collection, regulatory compliance, and ensuring that studies follow established protocols and guidelines.

Key Responsibilities:

• Coordinate and manage all aspects of clinical research studies from initiation to close-out 
• Recruit, screen, and enroll study participants according to protocol criteria 
• Obtain informed consent in compliance with ethical and regulatory standards 
• Schedule and conduct study visits, procedures, and follow-ups 
• Collect, record, and maintain accurate study data and source documentation 
• Ensure compliance with study protocols, institutional policies, and regulatory requirements (e.g., FDA, IRB, GCP) 
• Monitor participant safety and report adverse events as required 
• Maintain study files, regulatory binders, and case report forms 
• Communicate with investigators, sponsors, and study team members 
• Assist with audits and inspections by regulatory agencies 

Qualifications

• Bachelor’s degree in life sciences,  public health, or a related field 
• Experience in clinical research or healthcare (optional) 
• Knowledge of clinical trial regulations and guidelines (e.g., GCP, HIPAA) 
• Strong organizational and time-management skills 
• Excellent written and verbal communication skills 
• Attention to detail and ability to manage multiple tasks