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Clinical Research Program Manager

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LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA

Torrance, CA (In Person)

$107,500 Salary, Full-Time

Posted 3 weeks ago (Updated 2 weeks ago) • Actively hiring

Expires 6/3/2026

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Job Description

Clinical Research Program Manager
LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA
Torrance, CA Job Details $85,000 - $130,000 a year 1 day ago Qualifications Regulatory inspections Clinical research Research ethical considerations Adverse event reporting Compliance audits & assessments HIPAA Filing Mid-level Patient safety Schedule management Project management lifecycle Bachelor's degree Public Health Research compliance clinical trial records management Patient recruitment Bachelor's degree in public health Research regulatory compliance Data collection IRB compliance Healthcare data collection Communication skills FDA regulations Time management
Full Job Description 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

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