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Entry Level Clinical Research Associate Jobs in Minnesota

Children's Minnesota

Position Summary The primary responsibility of the Clinical Research Associate I (CRA I) is support of the research team in the conduct of department research projects. Responsibilities include but ...

HealthPartners

MN · On-site

$26.27 - $39.41/hr

... associate degree and at least one year research experience. * Licensure/ Registration ... ACRP Clinical Research Coordinator Certification desirable. * Knowledge, Skills, and Abilities:

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Entry Level Clinical Research Associate information

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How much do entry level clinical research associate jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for entry level clinical research associate in Minnesota is $27.74, according to ZipRecruiter salary data. Most workers in this role earn between $17.75 and $32.23 per hour, depending on experience, location, and employer.

What is an entry level clinical research associate?

An Entry Level Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory requirements, ethical guidelines, and study protocols. They assist in site selection, data collection, and verifying that study procedures are properly followed. Entry-level CRAs typically work under the supervision of senior CRAs and may travel to different clinical sites. Strong attention to detail, knowledge of Good Clinical Practice (GCP) guidelines, and organizational skills are essential. This role is a starting point for a career in clinical research, with opportunities for growth into senior CRA or project management positions.

What are the typical daily responsibilities of an entry level clinical research associate?

As an Entry Level Clinical Research Associate, your day-to-day work generally involves assisting with monitoring clinical trial sites, reviewing study documentation, and ensuring adherence to protocol and regulatory requirements. You may support more senior team members in conducting on-site or remote visits, tracking patient recruitment, and managing data collection. Additionally, you’ll communicate regularly with site staff and other stakeholders to resolve issues and ensure data quality. This hands-on experience is essential for building expertise in clinical research processes and advancing toward more senior CRA roles.

What are the key skills and qualifications needed to thrive as an entry level clinical research associate?

To thrive as an Entry Level Clinical Research Associate, you typically need a bachelor's degree in life sciences or a related field, a solid understanding of clinical trial protocols, and attention to detail. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory documentation is often required. Strong communication, organization, and problem-solving abilities help you effectively collaborate with study sites and team members. These skills are critical to ensure the accuracy, compliance, and successful progression of clinical studies.

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

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

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

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Entry Level Clinical Research Associate jobs near you
Infographic showing various Entry Level Clinical Research Associate job openings in Minnesota as of August 2026, with employment types broken down into 2% As Needed, 76% Full Time, 12% Part Time, and 10% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $57,693 per year, or $27.7 per hour.

Clinical Research Associate II

Minneapolis, MN • On-site

Inspire Medical Systems Inc.
Outpatient Health Care • 201 - 500 employees
Learn more about Inspire Medical Systems Inc.external

Full-time

Re-posted 5 days ago

Job description

POSITION SUMMARY 

This position is responsible for the initiation and independent oversight of clinical centers to ensure the successful conduct of active clinical studies. The Clinical Research Associate will ensure that clinical centers perform the clinical study according to the study protocol and regulatory standards by qualifying, training, monitoring, and overseeing study conduct at multiple clinical centers.

MAIN DUTIES/RESPONSIBILITIES 

  • Identify and assess the suitability of clinical study centers for participation in Inspire clinical trials. 
  • Serve as a primary point of contact for study sites, investigators, and other stakeholders. 
  • Train clinical centers on the clinical study protocol, data collection and good clinical practices. 
  • Communicate directly with clinical centers to maximize enrollment, ensure quality and timely data capture and answer study-related questions. 
  • Perform remote and on-site monitoring visits at participating clinical study centers to ensure the safety of study patients, the reporting of accurate study data and appropriate study management at the clinical study center. Ability to travel up to approximately 30% is required. 
  • Document site visits by preparing visit reports and follow-up letters to the clinical study centers. 
  • Facilitate effective communication and collaboration among study team members. 
  • Assist clinical centers with the preparation of IRB/EC submissions. 
  • Collect and archive study related documentation and correspondence. 
  • Communicate monitoring and site management updates to the internal clinical team. 
  • Assist with the development of the clinical study Monitoring Plan. 
  • Develop training materials and other study-related documentation. 
  • Maintain clinical monitoring tracking tools for each clinical study. 
  • Assist with other clinical related duties as assigned. 

QUALIFICATIONS 

Educational Requirements: 

  • High School Diploma or GED required 
  • Bachelor's Degree (BA or BS) preferred 
  • Science Degree preferred 

Required Experience: 

  • Previous experience in clinical research (minimum 3 years) 
  • Understanding of GCP and 21 CFR 812 
  • Experience with clinical documentation, clinical data and institutional review boards 

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