Clinical Research Program Manager

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 Background and Health Clearance Required Equal Opportunity Employer/Affirmative Action/Drug-Free Workplace #J-18808-Ljbffr