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Clinical Research Associate Jobs in Minnesota (NOW HIRING)

Mayo Clinic

Supervisor - Clinical Research

Rochester, MN · On-site

$87K - $124K/yr

The Clinical Research Supervisor is responsible for the coordination of all activities associated ... In lieu of Bachelor's degree, an Associate's degree with 7 years research experience or a high ...

Bio-Techne

Research Associate

Minneapolis, MN · On-site

$40K - $66K/yr

... and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to ... As a Research Associate in Luminex Operations, you will be responsible for supporting manufacturing ...

Bio-Techne

Research Associate

Minneapolis, MN · On-site

$40K - $66K/yr

... and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to ... As a Research Associate in Luminex Operations, you will be responsible for supporting manufacturing ...

Fairview Health Services

Research Nurse

Saint Paul, MN · On-site

$82 - $115/hr

Associate's Degree in Nursing Experience * 2 years clinical nursing experience * 2 years Clinical Research experience * 1-5 years research experience Preferred Education * BSN degree Experience

New

Fairview Health Services

Research Nurse

Saint Paul, MN · On-site

$81K - $115K/yr

Associate's Degree in Nursing Experience: * 2 years clinical nursing experience * 2 years Clinical Research experience * 1-5 years research experience Preferred Education: * BSN degree Experience:

Fairview Health Services

Research Nurse

Saint Paul, MN

$81K - $115K/yr

Associate's Degree in Nursing Experience: * 2 years clinical nursing experience * 2 years Clinical Research experience * 1-5 years research experience Preferred Education: * BSN degree Experience:

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How much do clinical research associate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical research associate in Minnesota is $40.28, according to ZipRecruiter salary data. Most workers in this role earn between $28.27 and $51.54 per hour, depending on experience, location, and employer.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

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

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

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

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
More about Clinical Research Associate jobs

What are the most commonly searched types of Clinical Research jobs in Minnesota?

The most popular types of Clinical Research jobs in Minnesota are:

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

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

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

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Cities in Minnesota with the most Clinical Research Associate job openings:

Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Minnesota as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $83,781 per year, or $40.3 per hour.

Clinical Research Coordinator

CENTER FOR VETERANS RESEARCH AND EDUCATION

Minneapolis, MN • On-site

$48K - $75K/yr

Full-time

Re-posted 15 days ago

Key responsibilities

  • Manage the day-to-day operations of multiple clinical research studies, including participant enrollment and data collection.

  • Oversee study activities, ensure regulatory compliance, and monitor participant progress and safety.

  • Coordinate study start-up, maintain study files and budgets, and serve as primary liaison with investigators, staff, and sponsors.

Job description


Job Title:           Clinical Research Coordinator

Location:          Minneapolis VA Medical Center

Job Code:          CRC, Full-Time, Benefits-Eligible, Exempt

Supervisor:    Principal Investigator

Project: 

Summary:

The Center for Veterans Research and Education (CVRE), whose mission is helping to support

innovative research and education initiatives that improve the health and well-being of Veterans, is

seeking a Clinical Research Coordinator

 

Position Description:

The Clinical Research Coordinator is responsible for the day-to-day operations of multiple clinical research studies. This position will actively enroll patients at the Minneapolis VA Medical Center.

Responsibilities: Major duties and responsibilities may include, but are not limited to the following:  

• Maintain close communication with local and network study leadership and staff. 

• Manage the study start-up process, including finalization of Informed Consent Forms 

   and preparation of study start-up materials. 

• Collaborate with the central Institutional Review Board overseeing VA sites, and the 

                  local Research and Development Committee (RDC), to ensure that regulatory 

                  requirements at the local site are identified, communicated, and observed. 

• Oversee enrollment and study activities with the Site Investigator. 

• Recruit participants, collect data in accordance with established study procedures, 

   follow up with participants in a timely manner. 

                • Dispense and track investigational study drug per protocol and in keeping with safe 

   medication handling practices. 

• Conduct phlebotomy and urine sample collection per study protocol. 

• Coordinate home visits between contract Home Health Service and study participants. 

• Monitor subjects' progress, including documentation and reporting of adverse events. 

• Ensure staff and subject compliance with protocol guidelines and requirements of 

   regulatory agencies. 

• Implement protocols to ensure data is collected in a scientifically valid manner. 

   Responsible for alerting the Site Investigator of data collection/protocol breeches, 

   inconsistencies, or other problems that may arise within the study, as well as suggesting 

   methods of correction. Maintain data and study files in accordance with study protocols. 

• Serve as primary liaison with Site Investigator, staff, internal/external resources and 

                   sponsor regarding patient care issues and progress of the study. 

• Maintain local budgets for the study; regularly report progress on all aspects of the 

   project to the Site Investigator. 

• Prepare documentation to support billing for this study’s sub-award, in cooperation 

   with CVRE staff. 

• Track expected and annual payments from the sponsor, in cooperation with CVRE staff.

• Ensure that study activities are completed in an ethical, culturally responsive, 

   scientifically rigorous, and timely manner in accordance with principles of Good Clinical 

• Other duties as assigned

 

Applicant must include a cover letter

 

Minimum Qualifications:

Education:   Bachelor’s Degree required (Master’s preferred)

 

Experience: 2-3 years of Research Assistant experience

0-2 years of Coordinator experience required for CRC I

2-4 years of Coordinator experience required for CRC II

                                                Preferred working knowledge of the study

Licensure/Registration/Certification: None

Knowledge, Skills, and Abilities:

  • Demonstrated ability to work effectively both independently and as part of a team.
  • Experience in coordinating multiple tasks and project elements with differing timelines and completion deadlines.
  • Excellent oral and written communication skills.
  • Exceptional attention to detail and organizational skills.
  • Proficiency in Microsoft Office products including Outlook, Word, PowerPoint and Excel.
  • Knowledge of Good Clinical Practice, human subjects’ protections, and federal regulations related to clinical research

 

Conditions of Employment:

  • Subject to a criminal and educational background check.
  • Designated and/or random drug testing may be required.
  • Regular and predictable attendance is required.
  • Typical hours fall within standard business hours, work may be required during hours beyond standard business hours, including weekends.
  • Must be a US citizen

Physical Requirements:  The employee must be able to navigate the medical center, use a keyboard, and life up to 25 lbs.  Reasonable accommodation may be considered in determining an applicant’s ability to perform the duties/functions of the position.