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Cra Clinical Research Associate Jobs in Wisconsin

Clinical Research Coordinator | Cardiology

Green Bay, WI ยท On-site

$23.50 - $31.25/hr

Certified Clinical Research Professionals (CCRP) Certification by Society of Clinical Research Associate (SOCRA) or Association of Clinical Research Professionals (ACRP) preferred. Minimum of three ...

Clinical Research Nurse Perform clinical assessments including blood pressure, venipuncture, weight ... Associate or Bachelor's degree in Nursing with current state licensure. CPR/AED certification. ACLS ...

Clinical Research Coordinator

Racine, WI

$22.75 - $30.25/hr

... and clinical aspects of multiple research projects. * Collaborate with primary investigator ... We empower our 99,000+ associates to bring their skills and expertise every day to reimagining ...

We empower our 99,000+ associates to bring their skills and expertise every day to reimagining ... and clinical aspects of multiple research projects. * Collaborate with primary investigator ...

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Cra Clinical Research Associate information

See Wisconsin salary details

$12

$41

$70

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

As of May 28, 2026, the average hourly pay for cra clinical research associate in Wisconsin is $41.51, according to ZipRecruiter salary data. Most workers in this role earn between $29.13 and $53.12 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate (CRA), and why are they important?

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 (CRAs) 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 are CRA Clinical Research Associates?

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.

Is it hard to get a CRA job?

Securing a CRA (Clinical Research Associate) position can be competitive due to the specialized skills required, such as knowledge of Good Clinical Practice (GCP) and clinical trial processes. Candidates often need relevant education, certifications, and experience in clinical research to improve their chances of obtaining the role.

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.

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What job categories do people searching Cra Clinical Research Associate jobs in Wisconsin look for? The top searched job categories for Cra Clinical Research Associate jobs in Wisconsin are:
What cities in Wisconsin are hiring for Cra Clinical Research Associate jobs? Cities in Wisconsin with the most Cra Clinical Research Associate job openings:
Infographic showing various Cra Clinical Research Associate job openings in Wisconsin as of May 2026, with employment types broken down into 1% As Needed, 65% Full Time, 30% Part Time, and 4% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $86,342 per year, or $41.5 per hour.
Remote Oncology Phase I Regional CRA (Belgium)

Remote Oncology Phase I Regional CRA (Belgium)

Advanced Clinical

Cedar Grove, WI โ€ข Remote

Full-time

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Advanced Clinical is looking for a Regional CRA to join their remote team, focusing on oncology clinical trials across Belgium. This permanent position requires fluency in both Dutch and French, with a minimum of 5 years CRA experience and a strong background in Phase I clinical trials. Key responsibilities include site monitoring, collaboration with investigators, and ensuring compliance with regulatory requirements.

Extensive travel (70-80%) is required. Join a dynamic environment and play a crucial role in advancing clinical research. #J-18808-Ljbffr