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.