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Entry Level Clinical Research Associate Jobs in Minnesota

Clinical Research Nurse - Pratt Cancer Center

Anoka, MN · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The study load and complexity will increase from the Associate Clinical Research Nurse responsibility, thereby increasing the overall number of enrollments and visits. The Clinical Research Nurse ...

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Entry Level Clinical Research Associate information

See Minnesota salary details

$10

$27

$57

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

As of Aug 15, 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 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 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 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:

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

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

What cities in Minnesota are hiring for Entry Level Clinical Research Associate jobs?

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

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, 78% Full Time, 14% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $57,693 per year, or $27.7 per hour.

Clinical Research Nurse - Pratt Cancer Center

Mercy

Anoka, MN • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 25 days ago


Mercy rating

6.5

Company rating: 6.5 out of 10

Based on 209 frontline employees who took The Breakroom Quiz

606th of 887 rated healthcare providers


Job description

Find your calling at Mercy!The Clinical Research Nurse (CRN) is responsible for coordination of research studies conducted by Mercy Research. The Clinical Research Nurse is responsible for the day-to-day operational tasks related to clinical trials and performs a variety of duties including, but not limited to, volunteer recruitment, drug/device/supply inventory maintenance, interaction with physicians, nurses, office staff, patients, and clinical monitors. Duties also include the collection, compilation, documentation and analysis of clinical research data while following local, state and federal regulations. The Clinical Research Nurse will assist in training and preceptor duties. The study load and complexity will increase from the Associate Clinical Research Nurse responsibility, thereby increasing the overall number of enrollments and visits. The Clinical Research Nurse will assist with communication and relationship building with sponsors and CROs.
Performs duties and responsibilities in a manner consistent with our mission, values, and Mercy Service Standards.Position Details:Clinical Research Nurse - OncologyLocation: Sindelar Cancer Center, 10050 Kennerly Road
Schedule: Full-Time, Day Shift

Overview

The Clinical Research Nurse (CRN) is a key member of the Mercy Research team, responsible for coordinating oncology clinical trials and ensuring compliance with all regulatory requirements. This role involves managing day-to-day operations of research studies, including patient recruitment, informed consent, data collection, and inventory control. The CRN collaborates with physicians, nurses, office staff, patients, and clinical monitors to deliver safe, efficient, and high-quality research services. Additional responsibilities include training new staff, supporting ministry-wide recruitment efforts, and building strong relationships with sponsors and CROs.

Key Responsibilities

  • Complete pre-study feasibility assessments and checklists accurately and on time.
  • Recruit and screen patients for eligibility; conduct informed consent discussions in a respectful and compliant manner.
  • Manage patient visits efficiently, including monitoring, interviews, and diagnostic evaluations.
  • Maintain accurate and timely documentation in case report forms and source documents.
  • Prepare and process specimens for laboratory analysis.
  • Educate patients on drug use, disease management, and self-monitoring.
  • Maintain inventory of study drugs, devices, and supplies.
  • Participate in internal quality control and compliance monitoring.
  • Assist with training new staff and supporting recruitment initiatives.
  • Serve as a liaison with sponsors, CROs, and community partners to promote research and patient enrollment.
  • Attend investigator meetings and training sessions as required (may involve travel).
  • Contribute to a collaborative and organized research office environment.

Qualifications

  • Education: Nursing Diploma, Associate's Degree in Nursing, or Bachelor's Degree in Nursing.
  • Licensure: Registered Nurse with a valid license in the state of practice.
  • Experience:
    • 2 years of nursing experience for candidates with a Bachelor's degree.
    • 3 years of nursing experience for candidates with an Associate's degree or diploma program.
    • Demonstrated experience may be gained through prior roles, completion of college degrees, or a combination of professional and educational experiences.
  • Other Knowledge, Skills, and Abilities:
    • Ability to perform basic patient assessments (e.g., vital signs, spirometry, ECGs, phlebotomy, blood glucose monitoring) or willingness to learn.
    • Excellent communication skills, especially in face-to-face interactions with healthcare professionals and patients.
    • Ability to interact respectfully and assertively with health professionals.
    • Working knowledge of computer applications, including Internet and Microsoft Office Suite.
    • Above-average proficiency in mathematics, including familiarity with the metric system.
    • Ability to work effectively both independently and in groups, with strong problem-solving skills.

Preferred Qualifications

  • Phlebotomy experience.
  • At least 2 years of clinical research experience.
Why Mercy?

From day one, Mercy offers outstanding benefits - including medical, dental, and vision coverage, paid time off, tuition support, and matched retirement plans for team members working 32+ hours per pay period.

Join a caring, collaborative team where your voice matters. At Mercy, you'll help shape the future of healthcare through innovation, technology, and compassion. As we grow, you'll grow with us.


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About Mercy

Sourced by ZipRecruiter

Our mission is clear. We bring to life a healing ministry through our compassionate care and exceptional service. At Mercy, we believe in careers that match the unique gifts of unique individuals - careers that not only make the most of your skills and talents, but also your heart.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Chesterfield, MO, US

Year founded

1827