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Clinical Study Associate Jobs in Minneapolis, MN

Abbott

Associate Clinical Data Manager

Maple Grove, MN · On-site

The Associate Clinical Data Manager is responsible for performing data management tasks within ... Translates Clinical Study requirements into technical requirements for eCRFs, edit checks, study ...

Abbott

Associate Clinical Data Manager

Maple Grove, MN · On-site

The Associate Clinical Data Manager is responsible for performing data management tasks within ... Translates Clinical Study requirements into technical requirements for eCRFs, edit checks, study ...

Coloplast

Clinical Trial Administrator

Minneapolis, MN · On-site

$65 - $85/hr

In performing these duties, the CTA works closely with Clinical Research Associates to support and provide guidance on the administration of all related aspects of a clinical study. The Clinical ...

Coloplast

Clinical Trial Administrator

Minneapolis, MN · On-site

$65K - $85K/yr

In performing these duties, the CTA works closely with Clinical Research Associates to support and provide guidance on the administration of all related aspects of a clinical study. The Clinical ...

Abbott

Sr. Clinical Quality Associate

Maple Grove, MN · On-site

... Clinical Quality Associate.This position could also bebased out ofourPlano, TXsite. THIS IS AN IN ... Study Support Review study documents for compliancetoapplicable regulations, standards, and ...

Abbott

Sr. Clinical Quality Associate

Maple Grove, MN · On-site

... Senior Clinical Quality Associate. This position could also be based out of our Plano, TX site ... Study Support • Review study documents for compliance to applicable regulations, standards, and ...

Abbott

Sr. Clinical Quality Associate

Maple Grove, MN · On-site

... Clinical Quality Associate.This position could also bebased out ofourPlano, TXsite. THIS IS AN IN ... Study Support Review study documents for compliancetoapplicable regulations, standards, and ...

Danaher

Principal Clinical Scientist

Chaska, MN · On-site +1

Our associates are involved in every stage of diagnostics, from ideation to development and ... You will drive strategic study designs, ensuring regulatory compliance, and achieving key ...

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All JobsClinical Study Associate JobsClinical Study Associate Jobs in Minneapolis, MN

Clinical Study Associate information

See Minneapolis, MN salary details

$13

$32

$57

How much do clinical study associate jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical study associate in Minneapolis, MN is $32.92, according to ZipRecruiter salary data. Most workers in this role earn between $22.07 and $43.41 per hour, depending on experience, location, and employer.

What is a clinical study associate?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

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

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.

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

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

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

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

What are the most commonly searched types of Clinical Study jobs in Minneapolis, MN?

The most popular types of Clinical Study jobs in Minneapolis, MN are:

Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in Minneapolis, MN as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 18% Part Time, and 8% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $68,477 per year, or $32.9 per hour.

Clinical Research Associate II

Inspire Medical Systems Inc.

Minneapolis, MN • On-site

Full-time

Re-posted 4 hours 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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