Clinical Research Program Manager
LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA
Behavioral Health Market Context
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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
- •3 more items(s)
Responsibilities
- •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
- •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
- •9 more items(s)
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