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

Please ensure your application is complete and signed; incomplete submissions will not be considered.

Background and Health Clearance Required

Equal Opportunity Employer/Affirmative Action/Drug-Free Workplace