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Clinical Study Assistant Jobs in Maple Grove, MN

Coloplast

Clinical Trial Administrator

Minneapolis, MN · On-site

$65 - $85/hr

The Clinical Trial Administrator (CTA) fulfils a specialized research role within the Clinical ... study-specific source documentation, regulatory binders and other materials * Assist principal ...

New

Coloplast

Clinical Trial Administrator

Minneapolis, MN · On-site

$65K - $85K/yr

The Clinical Trial Administrator (CTA) fulfils a specialized research role within the Clinical ... study-specific source documentation, regulatory binders and other materials * Assist principal ...

Coloplast Corp

Clinical Trial Administrator

Minneapolis, MN · On-site

$65K - $85K/yr

... study. The Clinical Trial Administrator is based in a Kerecis office and reports to the Director of Clinical Affairs. This is a full-time role. Major Areas of Accountability Assist in the preparation ...

New

Medtronic

Clinical Research Spec

Moundsview, MN · On-site +1

The Study & Scientific Solutions (S&SS) is a function within Medtronic Core Clinical Solutions (MC2). S&SS is an internal service provider to all of Medtronic and assigns resources to assist Business ...

Medtronic

Clinical Research Spec

Moundsview, MN · On-site +1

The Study & Scientific Solutions (S&SS) is a function within Medtronic Core Clinical Solutions (MC2). S&SS is an internal service provider to all of Medtronic and assigns resources to assist Business ...

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All JobsClinical Study JobsClinical Study Assistant JobsClinical Study Assistant Jobs in Maple Grove, MN

Clinical Study Assistant information

See Maple Grove, MN salary details

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How much do clinical study assistant jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical study assistant in Maple Grove, MN is $20.71, according to ZipRecruiter salary data. Most workers in this role earn between $16.97 and $23.89 per hour, depending on experience, location, and employer.

What is a clinical study assistant?

Clinical Study Assistants are professionals who support the conduct of clinical trials by handling administrative tasks, maintaining study documentation, and ensuring regulatory compliance. They work closely with clinical research teams to coordinate schedules, communicate with study sites, and help manage trial materials. Their role is crucial in ensuring that clinical studies run smoothly, efficiently, and according to protocols and regulatory guidelines.

What are the key skills and qualifications needed to thrive as a clinical study assistant?

To thrive as a Clinical Study Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or related fields, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation processes is typically required. Effective communication, teamwork, and problem-solving skills help you navigate complex study protocols and collaborate with diverse stakeholders. These abilities are crucial for ensuring the accuracy, compliance, and smooth operation of clinical research studies.

What are the main challenges a clinical study assistant might face when supporting clinical trial operations?

A Clinical Study Assistant often encounters challenges such as managing multiple tasks under tight deadlines, ensuring accurate documentation, and coordinating communication between research teams, sponsors, and regulatory bodies. Additionally, adapting to evolving study protocols and maintaining compliance with strict regulatory requirements can be demanding. Strong organizational skills, attention to detail, and proactive communication are essential for navigating these challenges successfully.

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

AspectClinical Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree, often with additional certifications in clinical research
Work EnvironmentSupports clinical trials in hospitals, research centers, or pharmaceutical companiesManages entire clinical studies, coordinating between sites, staff, and sponsors
Employer & IndustryHospitals, research institutions, pharmaceutical companiesAcademic medical centers, hospitals, research organizations
Search & Comparison IntentOften compared for entry-level roles supporting clinical trialsCompared for roles with broader responsibilities in clinical study management

The Clinical Study Assistant primarily supports clinical trial activities by assisting with data collection and documentation, while the Clinical Research Coordinator manages the overall conduct of the study, including patient recruitment and compliance. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

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

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

What cities near Maple Grove, MN are hiring for Clinical Study Assistant jobs?

Cities near Maple Grove, MN with the most Clinical Study Assistant job openings:

Clinical Study Assistant jobs near you
Infographic showing various Clinical Study Assistant job openings in Maple Grove, MN as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 17% Part Time, and 7% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $43,087 per year, or $20.7 per hour.

Clinical Research Associate II

Inspire Medical Systems Inc.

Minneapolis, MN • On-site

Full-time

Posted 29 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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