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Clinical Study Assistant Jobs in Michigan (NOW HIRING)

A.P.R., Inc. (AlphaProTemps)

Be Seen First

Clinical Research Coordinator (CRC)

Kalamazoo, MI · On-site

$44/hr

Maintain and update study files and records according to sponsor and institutional requirements ... * Assist in reviewing eligibility criteria for participant enrollment. * Coordinate enrollment of ...

Trice Healthcare

REGISTERD NURSE ICU

Bellaire, MI · On-site

Care for post-op open heart surgery patients, as well as those with congestive heart failure and undergoing electrophysiology studies. * Assist with national clinical trials managed by the NISUS ...

Tricehealthcare

REGISTERD NURSE ICU

Bellaire, MI · On-site

Care for post-op open heart surgery patients, as well as those with congestive heart failure and undergoing electrophysiology studies. * Assist with national clinical trials managed by the NISUS ...

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Clinical Study Assistant information

See Michigan salary details

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How much do clinical study assistant jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for clinical study assistant in Michigan is $17.63, according to ZipRecruiter salary data. Most workers in this role earn between $14.47 and $20.34 per hour, depending on experience, location, and employer.

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 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 most commonly searched types of Clinical Study jobs in Michigan? The most popular types of Clinical Study jobs in Michigan are:
Clinical Study Assistant jobs near you
Infographic showing various Clinical Study Assistant job openings in Michigan as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 19% Part Time, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $36,676 per year, or $17.6 per hour.

Clinical Research Assistant

McLaren Health Care Corp

Mount Pleasant, MI • On-site

Full-time

Posted 3 days ago

New

McLaren Health Care rating

6.7

Company rating: 6.7 out of 10

Based on 221 frontline employees who took The Breakroom Quiz

532nd of 887 rated healthcare providers

Job description

Position Summary:

Provides support to the clinical research coordinator or clinical research nurse. 

  Essential Functions and Responsibilities:

  1. Provides general administrative assistance, including but not limited to organizational processes, materials management and data entry support.
  2. Maintains files, logs and other materials in an organized, efficient manner.
  3. Assists clinical research staff to assure all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines.
  4. Updates the Clinical Trials Management System (CTMS).
  5. Responsible for obtaining required signatures on clinical trial documents and returning within specified time frames.
  6. Candidate will receive additional supportive mentoring for skills development after initial orientation.
  7. Assignments will be determined by supervisor based on skills, training and competence levels.     
  8. Assignments may broaden in complexity with experience requiring increasing self-directed activity.
  9. Responds to internal and external customer requests in a timely fashion.
  10. Assists with the coordination of sponsor visits.
  11. Performs data quality checks as needed.
  12. Performs other related duties as required and directed.

Qualifications:

Required:

  • High school diploma

Preferred: 

  • Six months experience with data entry.
  • Office experience in a medical setting.
Additional Information
  • Schedule: Full-time
  • Requisition ID: 26004377
  • Daily Work Times: 8am - 4:30pm
  • Hours Per Pay Period: 80
  • On Call: No
  • Weekends: No

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