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Regional Clinical Research Associate Jobs (NOW HIRING)

WEP Clinical

Senior Clinical Research Associate

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... SCRA II (5+ yrs) - oversees complex sites/regions, mentors peers, and drives process improvements

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

As a Clinical Research Associate at ICON , you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of ...

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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 8, 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 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 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 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 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.

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.

More about Regional Clinical Research Associate jobs
Who are the top companies hiring for Regional Clinical Research Associate jobs? The top employers for Regional Clinical Research Associate jobs are:
What states have the most Regional Clinical Research Associate jobs? States with the most job openings for Regional Clinical Research Associate jobs include:
What are popular job titles related to Regional Clinical Research Associate jobs? For Regional Clinical Research Associate jobs, the most frequently searched job titles are:
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 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

Clinical Research Associate l

University of Nebraska Medical Center

Omaha, NE • On-site

$18.99 - $28.51/hr

Full-time

Posted 9 days ago

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

52nd of 1,055 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_14904 Department Int Med Rheumatology 50000594 Business Unit College of Medicine Reg-Temp Full-Time Regular Work Schedule TBD by Supervisor and Responsibilities Remote/Telecommuting No remote/telecommuting opportunity Position Summary
The Research Associate will play a crucial role in the successful execution and completion of research studies within the UNMC Division of Rheumatology. This position involves coordinating various aspects of research projects, including IRB submissions, participant recruitment, study visits, data collection, and timely submission of study data to sponsors. The ideal candidate will have a strong work-ethic, familiarity with clinical research methodologies, excellent organizational skills, and the ability to work collaboratively within a multidisciplinary team.
Position Details
Additional Information
Posting Category Research - Non Academic Working Title Clinical Research Associate l 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 07/29/2026 Application Review Date 08/07/2026 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: Not Applicable Required Other Computer Applications: Required Additional Knowledge, Skills and Abilities:
Ability to work independently and as part of a team;
Ability to accurately follow study protocol guidelines;
Attention to detail in completing paperwork and data entry in a timely fashion;
Effective verbal and written communication skills; Effective organizational skills; Excellent verbal and written communication skills
Ability to identify potential problems.
Preferred Education: Relevant coursework/specialized training If any degree/training is preferred, please specify the type:
Training related to biological sciences, healthcare, laboratory and/or clinical research.
Preferred Experience: Preferred License: Yes If yes, what is the preferred licensure/certification?:
Phlebotomy certification, or willing to obtain.
Preferred Computer Applications: Preferred Other Computer Applications: Epic (Campus patient info system) Preferred Additional Knowledge, Skills and Abilities:
Have prior IRB and clinical research experience or be willing to be trained.
Email to a Friend https://unmc.peopleadmin.com/postings/99550

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