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Regional Clinical Research Associate Jobs (NOW HIRING)

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Clinical Research Associate

Long Beach, CA · On-site

$91K - $114K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Research Associate - Early Stage Development - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

410 ICR United States USA

$110K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Clinical Research Associate - Oncology (Myelofibrosis) - East Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

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$110K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Clinical Research Associate - Oncology (Myelofibrosis) - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

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Sr. Clinical Research Associate

Washington, DC

$110K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Clinical Research Associate - Oncology (Myelofibrosis) - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

Icon plc

Clinical Research Associate

Washington, DC

$91K - $114K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Research Associate - Early Stage Development - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

ICON

Clinical Research Associate

Long Beach, CA · On-site +1

$91K - $114K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Research Associate - Early Stage Development - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings Available* Position Location: 541 Church at North Hills St., Suite 1000, Raleigh, NC 27609 *100% Remote ...

Tigermed America

Clinical Research Associate

Denver, CO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Senior Clinical Research Associate As Clinical Research Associate you will be responsible for monitoring clinical trials and ensuring investigators are conducting the research within requirements of ...

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Senior Clinical Research Associate

Portland, OR · On-site

$110K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Clinical Research Associate - Oncology - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

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Senior Clinical Research Associate

Los Angeles, CA · On-site

$110K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Clinical Research Associate - Oncology - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

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Regional Clinical Research Associate information

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$11K

$79.4K

$137.5K

How much do regional clinical research associate jobs pay per year?

As of Aug 18, 2026, the average yearly pay for regional clinical research associate in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What is a regional clinical research associate?

A Regional Clinical Research Associate (CRA) is a professional responsible for monitoring clinical trials at sites within a specific geographic region. They ensure that clinical studies are conducted according to protocol, Good Clinical Practice (GCP) guidelines, and regulatory requirements. Regional CRAs act as a liaison between the clinical trial sponsor and research sites, performing site visits, verifying data accuracy, and ensuring patient safety. Their work helps ensure the integrity and reliability of clinical trial data while supporting the successful completion of research studies.

What does a regional clinical research associate do?

A regional clinical research associate works to manage studies and clinical trials associated with pharmaceutical and biotechnological drugs, products, and procedures. Your responsibilities in this career include writing and creating trial protocols, assisting in the scientific research that determines the efficacy and safety of vaccines or a medication, liaising with the ethics committee about trial subject safety, rights, and well-being, and training staff on protocol, case report form completion, and proper source documentation. Other duties include conducting research analysis, documenting and overseeing IP inventory, liaising with regulatory authorities, and tracking, managing, and ordering trial and IP materials.

What are the key skills and qualifications needed to thrive as a regional clinical research associate?

To thrive as a Regional Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory requirements, and a relevant life sciences degree, often complemented by industry experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are commonly required. Strong organizational, problem-solving, and communication skills help manage multiple sites, build rapport with investigators, and ensure protocol compliance. These competencies are critical for maintaining data integrity, ensuring regulatory compliance, and supporting successful clinical trial outcomes across diverse locations.

What are some common challenges regional clinical research associates face when managing multiple study sites?

Regional Clinical Research Associates (CRAs) often juggle overseeing several clinical trial sites, which can present challenges such as coordinating travel schedules, maintaining consistent communication with site staff, and ensuring all sites comply with study protocols and regulatory requirements. Balancing administrative duties with on-site monitoring visits requires strong organizational and time-management skills. Additionally, adapting to varying site cultures and addressing site-specific issues are essential for maintaining study quality and fostering effective collaboration.

What is the difference between Regional Clinical Research Associate vs Clinical Research Associate?

AspectRegional Clinical Research AssociateClinical Research Associate
Required CredentialsBachelor's degree, clinical research certification often preferredBachelor's degree, clinical research certification often preferred
Work EnvironmentTravel across multiple sites within a regionMonitor specific sites, often within a local area
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms
Search & Comparison IntentUnderstanding regional responsibilities and scopeMonitoring specific clinical trial sites

The main difference between a Regional Clinical Research Associate and a Clinical Research Associate lies in their scope of work. The Regional CRA oversees multiple sites within a region, often traveling extensively, while the CRA typically monitors individual sites within a specific area. Both roles require similar credentials and are employed in the same industry sectors, but their geographic focus and daily responsibilities differ.

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Regional Clinical Research Associate jobs near you
Infographic showing various Regional Clinical Research Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

Clinical Research Associate I

University of Nebraska Medical Center

Omaha, NE • On-site

$18.99 - $28.51/hr

Full-time

Re-posted yesterday

University Of Nebraska Medical Center rating

8.5

Company rating: 8.5 out of 10

Based on 15 frontline employees who took The Breakroom Quiz

55th of 1,060 rated hospitals

Job description

GENERAL REQUISITION INFORMATION
EEO Statement:
UNMC is an Equal Employment Opportunity Employer, including an equal opportunity employer of protected veterans and individuals with disabilities.
Location Omaha, NE Requisition Number: Staff_14495 Department Int Med DEM 50000586 Business Unit College of Medicine Reg-Temp Full-Time Regular Work Schedule As directed by supervisor Remote/Telecommuting No remote/telecommuting opportunity Position Summary
Provide clinical and administrative support for the division of DEM (Diabetes, Endocrinology and Metabolism) in the areas of clinical research and regulatory compliance. Support administrator with the processing of all IRB and regulatory paperwork. Duties will also include working with current and potential research subjects.
Position Details
Additional Information
Posting Category Research - Non Academic Working Title Clinical Research Associate I Job Title Clinical Research Associate L1 Salary Grade RA14H Appointment Type C2 - REG OFF/SERV HRLY Salary Range $18.990 - $28.510/hourly Job Requisition Begin Date 02/13/2026 Application Review Date 02/24/2026 Review Date Information:
Initial application review will begin on the date provided in the field above. Applications received prior to this review date will be considered. Applications received after the review date may be considered.
Required and Preferred Qualifications
Required Education: High School education or equivalent If any degree major/training is required, please specify the type. (NOTE: Concentration and minors are not equivalent to a major)
(Will consider three years related post high school education/experience)
Required Experience 3 years If any experience is required, please specify what kind of experience:
Experience related to healthcare, laboratory and/or clinical research
(Will consider three years related post high school education/experience)
Required License No If yes, what is the required licensure/certification? Required Computer Applications: Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Microsoft Outlook Required Other Computer Applications: Required Additional Knowledge, Skills and Abilities:
Exceptional organization skills.
Ability to communicate effectively both verbally and in writing.
Ability to prioritize and work independently.
Preferred Education: Relevant coursework/specialized training If any degree/training is preferred, please specify the type:
Training related to healthcare, laboratory and/or clinical research.
Preferred Experience: Preferred License: No If yes, what is the preferred licensure/certification?: Preferred Computer Applications: SAP, Microsoft Outlook Preferred Other Computer Applications: Electronic Health Records Preferred Additional Knowledge, Skills and Abilities: Email to a Friend https://unmc.peopleadmin.com/postings/96314

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