Job Description

Job Location: Torrance Campus - Torrance, CA 90502
Position Type: FT 80% - 32 hours per week (FT Benefit)
Salary Range: $85,000.00 - $130,000.00 Salary/year
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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:
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- - - - 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
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Qualifications
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- - - - 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
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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