Clinical Research Program Manager

LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA

Torrance, CAFull-timePosted Apr 28, 2026

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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