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Global Research Program Manager Jobs (NOW HIRING)

Wisconsin

PET/CT Research Program Manager

Madison, WI · Hybrid

Research Program Manager Job Summary: The Department of Radiology at the University of Wisconsin-Madison School of Medicine and Public Health is seeking an experienced, collaborative, and forward ...

Lionsgate

Director, Global Research

Santa Monica, CA · On-site

Monitor and evaluate global marketplace trends across broadcast, cable, FAST, AVOD, SVOD, and ... Proven leadership experience managing and developing teams * Exceptional presentation and ...

Virginia Tech

UPWARDS Program Manager

Blacksburg, VA · On-site

$35/hr

UPWARDS Program Manager Apply now Back to search results Job no: 537010 Work type: Hourly Wage ... A leading global research institution, Virginia Tech conducts more than $650 million in research ...

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How much do global research program manager jobs pay per year?

As of Sep 10, 2026, the average yearly pay for global research program manager in the United States is $125,543.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,500.00 and $137,500.00 per year, depending on experience, location, and employer.

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Infographic showing various Global Research Program Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $125,543 per year, or $60.4 per hour.

Clinical Research Program Manager

Torrance, CA • On-site

LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA
See more jobs at LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLAexternal

Full-time

Re-posted 14 days ago

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

Apply