Clinical Research Program Manager
Job
LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA
Torrance, CA (In Person)
$107,500 Salary, Full-Time
Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
100
out of 100
Average of individual scores
Skill Insights
Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.
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 managementFull 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 WorkplaceSimilar jobs in Torrance, CA
TEKsystems c/o Allegis Group
Torrance, CA
Posted2 days ago
Updated12 hours ago
Careers Integrated Resources Inc
Torrance, CA
Posted2 days ago
Updated12 hours ago
Similar jobs in California
ActionLink
West Hollywood, CA
Posted2 days ago
Updated12 hours ago
TRAFFIC MANAGEMENT, LLC
Long Beach, CA
Posted2 days ago
Updated12 hours ago