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Ucla Clinical Research information

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$49K

$107.3K

$189K

How much do ucla clinical research jobs pay per year?

As of Aug 6, 2026, the average yearly pay for ucla clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a UCLA Clinical Research professional?

To thrive as a UCLA Clinical Research professional, you need a strong background in biomedical sciences, research methodology, and regulatory compliance, often supported by a bachelor’s or master’s degree in a health-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and relevant certifications such as CCRC or CCRP are typically required. Excellent organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating studies and collaborating with multidisciplinary teams. These competencies ensure the integrity, safety, and efficiency of clinical research projects, contributing to high-quality outcomes and compliance with regulatory standards.

What is a UCLA Clinical Research?

A UCLA Clinical Research position typically involves working on medical studies that aim to advance healthcare by studying new treatments, medications, or medical devices. Professionals in these roles may recruit patients, collect and analyze data, ensure compliance with research protocols, and support principal investigators. These positions are essential for translating scientific discoveries into better patient care, and they often require strong organizational, communication, and analytical skills. At UCLA, clinical research staff contribute to groundbreaking projects in collaboration with world-renowned clinicians and scientists.

What is the difference between Ucla Clinical Research vs Clinical Research Coordinator?

AspectUcla Clinical ResearchClinical Research Coordinator
Required CredentialsBachelor's degree, clinical research certifications often preferredBachelor's degree, certifications like CCRP beneficial
Work EnvironmentAcademic medical centers, university-affiliated research settingsHospitals, clinics, research sites
Employer & IndustryUCLA, academic institutions, research organizationsHospitals, research institutions, pharmaceutical companies
Common Search & ComparisonYesYes

Ucla Clinical Research roles typically involve working within academic and university settings, focusing on clinical trials and research studies. Clinical Research Coordinators (CRCs) often work across various healthcare environments, managing day-to-day trial activities. While both roles require similar educational backgrounds and certifications, Ucla Clinical Research positions are more associated with academic research projects, whereas CRCs are more broadly employed in clinical settings.

What are some common challenges faced by clinical research staff at UCLA, and how can applicants prepare to address them?

Clinical research staff at UCLA often manage multiple studies simultaneously, each with its own protocols and deadlines. Navigating complex regulatory requirements while maintaining strict ethical standards is a key challenge. Applicants can prepare by familiarizing themselves with clinical trial regulations, honing their organizational skills, and developing strong communication abilities to effectively coordinate with principal investigators, sponsors, and participants. Proactively seeking training in Good Clinical Practice (GCP) and staying current with institutional policies can also be beneficial.
More about Ucla Clinical Research jobs
What cities are hiring for Ucla Clinical Research jobs? Cities with the most Ucla Clinical Research job openings:
What states have the most Ucla Clinical Research jobs? States with the most job openings for Ucla Clinical Research jobs include:
What job categories do people searching Ucla Clinical Research jobs look for? The top searched job categories for Ucla Clinical Research jobs are:
Ucla Clinical Research jobs near you
Infographic showing various Ucla Clinical Research job openings in the United States as of August 2026, with employment types broken down into 80% Full Time, and 20% Part Time. Highlights an 100% In-person job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Unit Supervisor

UCLA Health

Los Angeles, CA

$86K - $184K/yr

Full-time

Re-posted 6 days ago

UCLA Health rating

8.7

Company rating: 8.7 out of 10

Based on 136 frontline employees who took The Breakroom Quiz

6th of 887 rated healthcare providers

Job description

Description

The Department of Medicine is seeking a Clinical Research Unit Supervisor at the UCLA Clinical AIDS Research and Education (CARE) Center to lead and oversee the coordination of HIV and other infectious diseases. In this role, you will provide direct supervision to research staff and ensure the smooth operation of study activities from design and setup through conduct and closeout. You will manage unit operations to guarantee compliance with departmental policies, organizational standards, and regulatory requirements, including FDA Code of Federal Regulations (CFR), ICH Good Clinical Practice (GCP), and institutional procedures.

As a key liaison, you will collaborate with Principal Investigators, sponsors, central research infrastructure teams, ancillary departments, and other stakeholders to support all aspects of study administration—including compliant study conduct, financial oversight, and personnel management. Your leadership will ensure studies are executed efficiently, ethically, and in full alignment with protocol and regulatory guidelines.

This role offers the opportunity to make a meaningful impact on research operations while mentoring a team and supporting high-quality clinical research within the Department of Medicine.

Annual range: $86,400-$184,800

Qualifications

Required:

  • Bachelor’s Degree in related area and or equivalent experience. Advanced degree preferred
  • Minimum of 5+ years of experience in a clinical research setting
  • Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as a member of a team.
  • Analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actions.
  • Demonstrated proficiency with Adobe and Microsoft suite software, especially Excel and Word, to perform daily tasks efficiently and accurately.  Ability to learn additional systems, including DocuSign, Florence eBinders, and others as needed.
  • Knowledge of and experience working with a variety of local and external IRBs, scientific review and other research committees, national cooperative group sponsors, industry sponsors, federal and foundation funding organizations, etc.
  • Ability to handle confidential information with judgement and discretion.
  • Availability to work in more than one environment, travelling to various clinic sites, meetings, conferences, etc, including out of state network and investigator meetings.
  • Demonstrated ability to interpret IRB, FDA, federal and UCLA requirements and utilize that information to guide investigators and other team members.
  • Expert level working knowledge of clinical research concepts, policies and procedures, and human safety protection regulations and laws.
  • Demonstrated experience and knowledge of clinical trials budgeting processes to manage the preparation of clinical trials budgets.
  • Demonstrated experience with FDA processes and procedures.
  • Ability to lead the development and implementation of quality improvement activities, SOPs, processes, etc.
  • Team leadership experience (i.e. projects, committees, etc.).
  • Ability to develop and give presentations to leadership, positively representing the department.
  • Ability to predict potential problems and proactively implement solutions.
  • Ability to clearly communicate complex departmental and institution-wide policies and ensure understanding.
  • Ability to manage complex and sometimes conflicting departmental priorities and external timelines.
  • Previous supervisory experience

Preferred:
  • Clinical Research Certification (CCRP, ACRP, etc.)
  • Experience with laboratory standards and functions including Good Clinical Laboratory Practice (GCLP)
  • Experience with HIV and/or other infectious disease clinical trials
  • Working knowledge and understanding of NIH Division of AIDS (DAIDS) policies, procedures, and operations
  • Demonstrated ability to prepare for, facilitate, and respond to site monitoring visits and audits in compliance with FDA, GCP, ICH guidelines, and sponsor requirements.
  • Familiarity with grant and other report writing

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About UCLA Health

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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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