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Research Coordinator Supervisor Jobs (NOW HIRING)

RWJBarnabas Health

Research Coordinator

Livingston, NJ · On-site

$35 - $40/hr

Research Coordinator Location: Melchiorre Cancer Center Department Name: Cancer Ctr-Research Req ... Actively identifies, addresses, and communicates to study team and supervisor any challenges with ...

RWJBarnabas Health

Research Coordinator

Livingston, NJ · On-site

$35 - $40/hr

Research Coordinator Location: Melchiorre Cancer Center Department Name: Cancer Ctr-Research Req ... Actively identifies, addresses, and communicates to study team and supervisor any challenges with ...

Pinnacle Clinical Research

WI · On-site

$22.25 - $29.50/hr

Clinical Research Coordinator Full Time Houston, TX, US 23 days ago Requisition ID: 1074 Summary ... Complete documentation and data management-related tasks as instructed by supervisor and compliance ...

Pinnacle Clinical Research

$22.75 - $30.25/hr

Clinical Research Coordinator II Full Time Professional Framers Branch, TX, US 7 days ago ... Complete documentation and data management related tasks as instructed by supervisor and compliance ...

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How much do research coordinator supervisor jobs pay per year?

As of Sep 11, 2026, the average yearly pay for research coordinator supervisor in the United States is $80,570.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,000.00 and $99,500.00 per year, depending on experience, location, and employer.

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Infographic showing various Research Coordinator Supervisor job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $80,570 per year, or $38.7 per hour.

Clinical Research Supervisor/Coordinator - Pediatrics

Los Angeles, CA • On-site

UCLA Health
Health Care and Social Assistance • 10K+ employees
Learn more about UCLA Healthexternal

$88K - $190K/yr

Full-time

Re-posted 20 hours ago

Key responsibilities

  • Oversee, coordinate, and manage complex investigational drug clinical trials.

  • Supervise and support clinical research coordinators, including managing staff schedules, providing training, and mentorship.

  • Participate in study implementation, participant recruitment, data collection, and monitoring to ensure compliance with regulations and high data quality.

UCLA Health rating

8.7

Company rating: 8.7 out of 10

Based on 137 frontline employees who took The Breakroom Quiz

Job description

General Information
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Work Location: Los Angeles, CA, USA
Onsite or Remote
Flexible Hybrid
Work Schedule
Monday-Friday, 8:00am-5:00pm - Flexibility required
Posted Date
07/14/2026
Salary Range: $88900 - 190300 Annually
Employment Type
2 - Staff: Career
Duration
indefinite
Job #
31885
Primary Duties and Responsibilities
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The Department of Pediatrics Clinical Research Excellence at Work (CREW) Clinical Research Coordinator Supervisor is an experienced professional responsible for overseeing, coordinating, and managing complex investigational drug clinical trials, as well as supervising other clinical research coordinators. This role involves close collaboration with principal investigators, study sponsors, university administrators, and regulatory agencies to ensure efficient study operations while upholding high standards for data quality, participant safety, and overall experience. The CREW Clinical Research Coordinator Supervisor plays a key role in addressing operational challenges, supporting staff development, and contributing to process improvement initiatives and corrective action plans. They help ensure the integrity of clinical trials by participating in study implementation, participant recruitment, data collection and monitoring, and maintaining compliance with institutional policies, Good Clinical Practice (GCP), and applicable federal regulations. In addition, the CREW Clinical Research Coordinator Supervisor oversees the daily activities of clinical research coordinators to ensure studies are conducted efficiently and in compliance with all requirements. Core supervisory responsibilities include managing staff schedules, providing training and mentorship while reinforcing adherence to institutional policies and regulatory standards, GCP and FDA regulations.
Salary Range: $88,900.00 - 190,300.00 Annually
Job Qualifications
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Required:
  • Bachelor's degree and/or equivalent combination of education and experience.
  • A minimum of 3 years prior experience in professional postgraduate clinical research coordination
  • Prior experience with a clinical research management system such as OnCore. Prior experience using an electronic health record such as Epic for clinical research purposes.
  • Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, participant recruitment and retention, data reporting, etc.
  • Strong working knowledge of Good Clinical Practices (GCP), the International Council for Harmonization and US federal guidelines and regulations for clinical research.
  • Prior experience with interventional investigational drug clinical trials.
  • Strong communication skills and experience working with cross functional teams.
  • Strong computer skills including use of Word, Excel, PowerPoint, Outlook, Adobe, e-mail and databases to create reports, correspondence and other documents as required.
  • Capable of multi-tasking and managing deadlines, balancing assignments from multiple individuals.
  • Demonstrated understanding of confidential information, how it is defined, and demonstrated skill in maintaining confidential status of such information.
  • Willingness to maintain a positive, determined attitude in achieving difficult objectives in a dynamic, complex, ever-evolving work environment.
  • Demonstrated interpersonal and communication skills to work with patients, their families/ guardians, physicians, administrators, work colleagues, representatives from sponsors and others to achieve maximum efficiency in reaching and maintaining workplace goals in a professional manner.
  • Skill in preparation of accurate and timely reports and statistical information on all protocols as needed.

Preferred:
  • Certificate in clinical research administration such as CCRP, ACRP, or equivalent.
  • Prior supervisory or mentorship experience.
  • Previous experience working with a range of clinical research specialty content areas and sponsors including NIH and industry sponsored trials. Experience conducting clinical research involving

As a condition of employment, the final candidate who accepts an offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; or have filed an appeal of a finding of substantiated misconduct with a previous employer.
Current/former UC employees are subject to a personnel file review.

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About UCLA Health

Sourced by ZipRecruiter

UCLA Health, operating within the healthcare industry, is significantly recognized for its commitment to improving the health and wellbeing of people through the integration of patient care, research, and education. Located in Los Angeles, California, UCLA Health was founded and associated with the University of California, Los Angeles (UCLA) in 1955, entrenching its roots in quality healthcare service provision. Through a broad range of medical services, UCLA Health significantly stands as a cornerstone for comprehensive outpatient, inpatient, and emergency care services, specialized treatments, and wellness checks. Notable for pioneering an integrated, comprehensive medical approach, UCLA Health is consistently ranked among the top health systems in the US and world.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Los Angeles, CA, US

Year founded

1955

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