Be an Early Applicant
90502, Torrance, CA, USA
In-Office
85K-130K Annually
Entry level
Healthtech • Social Impact • Biotech • Pharmaceutical
The Role
The Clinical Research Program Manager coordinates clinical trials, ensuring compliance with protocols, recruiting participants, and managing study data and communication.
Summary Generated by Built In

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


Skills Required

  • Bachelor's degree in life sciences, public health, or a related field
  • Experience in clinical research or healthcare
  • 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
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The Company
HQ: Torrance, CA
Year Founded: 1952

What We Do

The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center is a leading nonprofit research organization focused on biomedical innovation, translating discovery into health impact through research, education, and community outreach.

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