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Study Coordinator Jobs in Minnesota (NOW HIRING)

NAMSA

Associate Study Coordinator-ISR

Minneapolis, MN · On-site

$24/hr

Assists in the coordination of study tasks from pre-study initiation to study completion. Performs accurate and timely record keeping consistent with the maintenance of facility SOPs. Utilizes ...

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Study Coordinator information

See Minnesota salary details

$21.5K

$53.7K

$78.8K

How much do study coordinator jobs pay per year?

As of Aug 19, 2026, the average yearly pay for study coordinator in Minnesota is $53,724.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,100.00 and $61,200.00 per year, depending on experience, location, and employer.

What is a study coordinator?

A study coordinator works in a clinical research environment. In this position, your job duties are to oversee the day-to-day operations of a given study under the guidance of a research director. You direct tests, ensure all research is done according to ethical standards, and ensure the comfort and safety of subjects. As a study coordinator, you also ensure all patients provide informed consent prior to participation. Overall, your responsibility is to provide a safe environment for the study. To be a study coordinator, the qualifications are usually a bachelor’s degree or an RN degree. You typically need several years of experience in a clinical setting, and you must demonstrate skills in research.

What are the key skills and qualifications needed to thrive as a study coordinator, and why are they important?

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, usually backed by a bachelor’s degree in a science or health-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, attention to detail, and effective communication help you manage study logistics and collaborate with research teams and participants. These skills ensure that studies are conducted ethically, efficiently, and in accordance with regulatory standards.

What are some common challenges study coordinators face when managing multiple clinical trials simultaneously?

Study Coordinators often juggle several clinical trials at once, each with its own protocols, timelines, and regulatory requirements. Keeping track of participant enrollment, data collection, and compliance across different studies can be demanding and requires strong organizational skills. Effective communication with investigators, sponsors, and other team members is crucial to prevent errors, ensure deadlines are met, and maintain the quality of study data. Using robust tracking systems and prioritizing tasks can help manage these challenges efficiently.

What is the difference between Study Coordinator vs Research Assistant?

AspectStudy CoordinatorResearch Assistant
Required CredentialsTypically a bachelor's degree in health sciences, biology, or related fieldOften a bachelor's degree or current student in a related field
Work EnvironmentClinical research settings, hospitals, or research institutionsLaboratories, research centers, or clinical sites
Employer & Industry UsageUsed by hospitals, universities, and research organizationsCommonly employed in academic and research institutions
Common Search & Comparison IntentUnderstanding roles, responsibilities, and qualificationsLearning about entry-level research roles and support tasks

The Study Coordinator and Research Assistant roles share similarities in working within research environments and requiring related educational backgrounds. However, Study Coordinators typically have more responsibilities in managing study protocols and participant coordination, while Research Assistants focus on supporting research activities and data collection. Both roles are essential in advancing clinical research and often work closely together in research projects.

How much does a study coordinator make?

The average salary for a study coordinator in California is approximately $60,000 to $75,000 per year, depending on experience, education, and the specific healthcare or research setting. Salaries can vary based on certifications, such as CRC or CCRP, and the complexity of the studies managed.

What qualifications do you need to be a research study coordinator?

A research study coordinator typically needs a bachelor's degree in a health-related field such as nursing, biology, or psychology. Relevant experience in clinical research, strong organizational skills, and knowledge of regulatory requirements like Good Clinical Practice (GCP) are also important; some positions may require certification such as the Certified Clinical Research Coordinator (CCRC).
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What are the most commonly searched types of Study jobs in Minnesota?

The most popular types of Study jobs in Minnesota are:

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For Study Coordinator jobs in Minnesota, the most frequently searched job titles are:

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The top searched job categories for Study Coordinator jobs in Minnesota are:

What cities in Minnesota are hiring for Study Coordinator jobs?

Cities in Minnesota with the most Study Coordinator job openings:

Study Coordinator jobs near you
Infographic showing various Study Coordinator job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $53,724 per year, or $25.8 per hour.

Study Coordinator

Element Research Group Inc

Minneapolis, MN • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 10 days ago

Job description

Description:

Element Research Group (ERG) is a Preclinical Contract Research Organization specializing in functional and performance testing of medical devices, biologics, and drugs throughout all therapeutic areas.

This type of testing can include proof-of-concept, feasibility, demonstrating efficacy though subjective assessment or though statistically powered hypotheses, and demonstrating safety of a particular device or therapy. Performance testing is conducted in animal research models that are anatomically suitable to implant a device and evaluate its use as it is intended to ultimately be used in humans. These tests are often custom designed based on the experience of investigators, available literature, and specific goals for the study.

The study coordinator position is a supportive role to study directors conducting nonclinical studies at ERG. Study coordinators will contribute to the organization and execution of the technical conduct of study procedures, documentation and data collection, and reporting of results.


Element Research Group in located in Brooklyn Park, MN and this is an on-site role with 1 day remote. ERG offers comprehensive medical, dental and vision benefits with additional HSA company contribution, 401K matching, and PTO. Salary range competitive within the med/tech Twin Cities Market.


Job Duties:

  • Assist in the development of protocol specific data sheets for essential data capture during the conduct of nonclinical testing.
  • Provide medical research services throughout the duration of assigned nonclinical testing as requested by the study director
  • Provide consistent, timely, and detailed communication with the client, Element Research Group employees, and various test sites throughout the conduct of a study as requested by the study director.
  • Assist in project management of assigned nonclinical studies such as management of external test sites/contractors and ordering study-specific supplies.
  • Serve as Principal Investigator for studies in which ERG functions as a test site as requested by Test Facility Management or designee.
  • Assist in providing protocol training prior to and/or during study activities for nonclinical studies, as needed.
  • Assist in the identification and reporting of study deviations.
  • Assist in returning study materials to sponsors or archival of study files after study completion or closure.
  • Other tasks as assigned by Testing Facility Management or designee.

Seniority Level will be based on years of experience:

Study Coordinator I: Less than 1 year of study coordinator or related preclinical experience.

Study Coordinator II: Demonstrated proficiency as a study coordinator in complex nonclinical studies and greater than 1 year experience in study coordinator position.

Study Coordinator III: Demonstrated proficiency as a study coordinator in complex nonclinical studies and greater than 3 years experience in study coordinator position.



Requirements:

Education/Experience:

Associates or Bachelor’s Degree in a scientific field

Prior nonclinical research experience is preferred

Experience and applied knowledge may be considered in lieu of a degree


Technical Experience/Knowledge:

Knowledge Good Laboratory Practices guidelines as well as accepted testing standards such as ISO 10993 Biological Evaluation of Medical Devices and other available guidance documents

Ability to communicate effectively with scientists, veterinary care professionals, engineers, physicians, and key opinion leaders

Working knowledge of comparative anatomy and physiology (human and veterinary anatomy), medical procedures, and the function of medical devices

Strong attention to detail and organizational skills

Proficiency in Microsoft Office