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Clinical Monitoring Associate Jobs in Minnesota (NOW HIRING)

I-LUMEN SCIENTIFIC INC

Sr. CRA

Minneapolis, MN · On-site

Building for a better tomorrow. i-Lumen is seeking a Senior Clinical Research Associate (Sr. CRA ... Perform site monitoring visits including close-out (on-site and remote) in accordance with the ...

Abbott

Sr. Clinical Quality Associate

Maple Grove, MN · On-site

Whetherit'sglucose monitoring systems, innovative therapies for treating heart disease, or products ... Clinical Quality Associate.This position could also bebased out ofourPlano, TXsite. THIS IS AN IN ...

Abbott

Sr. Clinical Quality Associate

Maple Grove, MN · On-site

Whetherit'sglucose monitoring systems, innovative therapies for treating heart disease, or products ... Clinical Quality Associate.This position could also bebased out ofourPlano, TXsite. THIS IS AN IN ...

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Clinical Monitoring Associate information

See Minnesota salary details

$12

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$54

How much do clinical monitoring associate jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical monitoring associate in Minnesota is $30.89, according to ZipRecruiter salary data. Most workers in this role earn between $20.72 and $40.72 per hour, depending on experience, location, and employer.

What is a clinical monitoring associate?

Clinical Monitoring Associates (CMAs) are professionals who support the conduct of clinical trials by assisting with the monitoring of study sites to ensure compliance with protocols, regulatory requirements, and good clinical practice guidelines. They work closely with Clinical Research Associates and study coordinators to track the progress of trials, verify data accuracy, and manage documentation. CMAs play a crucial role in maintaining data integrity and patient safety throughout the clinical research process.

How does a clinical monitoring associate typically collaborate with clinical research teams during a study?

Clinical Monitoring Associates (CMAs) work closely with clinical research teams, including Clinical Research Associates (CRAs), project managers, and site staff. They support the coordination of study activities by tracking site progress, preparing essential documentation, and helping resolve site queries. CMAs often participate in regular team meetings, communicate updates, and ensure accurate data collection and compliance with study protocols. This collaborative environment helps ensure that clinical trials run smoothly and meet regulatory requirements.

What are the key skills and qualifications needed to thrive as a clinical monitoring associate, and why are they important?

To thrive as a Clinical Monitoring Associate, you need a background in life sciences, familiarity with Good Clinical Practice (GCP) guidelines, and a relevant bachelor's degree. Experience with clinical trial management systems (CTMS), electronic data capture (EDC), and certifications in clinical research (such as ACRP or SOCRA) are often required. Strong attention to detail, organizational skills, and effective communication help you excel in site management and ensure protocol adherence. These competencies are crucial for maintaining regulatory compliance, ensuring patient safety, and supporting the successful execution of clinical trials.

What cities in Minnesota are hiring for Clinical Monitoring Associate jobs?

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

Clinical Monitoring Associate jobs near you

Clinical Research Associate II

Inspire Medical Systems Inc.

Minneapolis, MN

Full-time

Re-posted 4 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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