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How much do cra clinical research associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for cra clinical research associate in Nebraska is $39.21, according to ZipRecruiter salary data. Most workers in this role earn between $27.50 and $50.19 per hour, depending on experience, location, and employer.

What is a clinical research associate?

CRA Clinical Research Associates are professionals who monitor clinical trials to ensure they are conducted in accordance with regulatory requirements, study protocols, and Good Clinical Practice guidelines. They act as a bridge between the sponsor of a clinical trial and the sites where the trial is conducted, overseeing data collection, patient safety, and compliance. Their responsibilities include site visits, reviewing documentation, and ensuring accurate reporting of study results. CRAs play a critical role in advancing medical research by maintaining the integrity and quality of clinical studies.

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

To thrive as a Clinical Research Associate (CRA), you need a solid background in life sciences, experience in clinical trial monitoring, and typically a bachelor's degree in a related field. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory requirements is essential, and certifications like ACRP or SOCRA are often advantageous. Strong attention to detail, organizational skills, effective communication, and adaptability help CRAs excel in coordinating studies and collaborating with diverse stakeholders. These skills ensure clinical trials are conducted ethically, efficiently, and in compliance with regulatory standards, safeguarding both data integrity and patient safety.

What are some common challenges faced by clinical research associates when managing multiple clinical trial sites?

CRAs often juggle oversight of multiple clinical trial sites, which can present challenges such as coordinating visits, ensuring consistent protocol adherence, and managing varying site performance. Effective communication and strong organizational skills are crucial, as CRAs need to address site-specific issues, maintain accurate documentation, and ensure timely data collection. Additionally, adapting to diverse team dynamics and staying updated with regulatory requirements across sites are common aspects of the role. Employers typically provide training and support, but successful CRAs proactively develop strategies to manage these complexities.

What is the difference between Cra Clinical Research Associate vs Clinical Trial Coordinator?

AspectCra Clinical Research AssociateClinical Trial Coordinator
CredentialsTypically requires a bachelor's degree in life sciences, nursing, or related field; certifications like CCRP or RAC are commonUsually holds a bachelor's degree in health sciences, nursing, or related field; certifications like CCRP are also beneficial
Work EnvironmentWorks primarily on-site at clinical trial sites, monitoring study progress and complianceCoordinates trial activities, manages schedules, and ensures protocol adherence, often working at trial sites or offices
Employer & IndustryEmployed by pharmaceutical companies, CROs, or research institutions in the clinical research industryEmployed by hospitals, research centers, or pharmaceutical companies to manage trial logistics

While both roles support clinical trials, Cra Clinical Research Associates focus on monitoring and compliance, whereas Clinical Trial Coordinators handle trial logistics and coordination. Both require relevant certifications and work in similar environments within the clinical research industry.

What are popular job titles related to Cra Clinical Research Associate jobs in Nebraska?

For Cra Clinical Research Associate jobs in Nebraska, the most frequently searched job titles are:

What job categories do people searching Cra Clinical Research Associate jobs in Nebraska look for?

The top searched job categories for Cra Clinical Research Associate jobs in Nebraska are:

What cities in Nebraska are hiring for Cra Clinical Research Associate jobs?

Cities in Nebraska with the most Cra Clinical Research Associate job openings:

Cra Clinical Research Associate jobs near you
Infographic showing various Cra Clinical Research Associate job openings in Nebraska as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $81,560 per year, or $39.2 per hour.

Postdoctoral Research Associate

University of Nebraska Medical Center

Omaha, NE • On-site

Full-time

Re-posted 29 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

54th of 1,065 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: 2026 - 289 Department COP Pharmaceutical Science 50000722 Business Unit(College/Institute) College of Pharmacy FTE:
100
Reg-Temp Full-Time Regular Work Schedule M-F 8am-5pm Requisition Category Research - Academic Requisition Title Postdoctoral Research Associate Job Title/Academic Rank Postdoctoral Research Associate Additional Requisition Title Appointment Type A1 - REG OTHER ACAD SAL Salary Range Salary Commensurate with Experience Job/EEO Category Professional Non-Faculty (Includes Other Academic) Job Requisition Begin Date 07/17/2026
Position Qualification
Position Summary
The Sun Lab in the College of Pharmacy at the University of Nebraska Medical Center (UNMC) is seeking motivated postdoctoral research associate with background in chemistry, nanomedicine, gene/drug delivery or cancer therapy. We are dedicated to designing and developing nanocarriers for the effective delivery of small molecule drugs and/or therapeutic genes (such as siRNA, plasmids, mRNA) for the treatment of cancer and other diseases; developing new strategies to overcome major clinical translation barriers in nanomedicine; and exploring the potential mechanisms using bioinformatics and molecular biology methods. The candidate will be responsible for using chemical tools to develop new nanocarriers with low toxicity and high delivery efficacy, and tackle the problems in the treatment of cancer.
Required Qualifications
PhD
Supplemental Qualifications

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