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Trials Manager Jobs in Michigan (NOW HIRING)

Insight

Research Executive Assistant

Flint, MI · On-site

$18.75 - $25.75/hr

This role requires hands-on experience in clinical research/clinical Trials and a strong ... Manage complex calendars, meeting coordination, and travel arrangements for research leadership

Insight

Research Executive Assistant

Detroit, MI · On-site

$19 - $26.25/hr

This role requires hands-on experience in clinical research/clinical Trials and a strong ... Key Responsibilities: • Manage complex calendars, meeting coordination, and travel arrangements ...

Insight

Research Executive Assistant

Flint, MI · On-site

$18.75 - $25.75/hr

This role requires hands-on experience in clinical research/clinical Trials and a strong ... Key Responsibilities: • Manage complex calendars, meeting coordination, and travel arrangements ...

McLaren

Clinical Research Coordinator II

Detroit, MI · On-site

$24 - $32/hr

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the ...

McLaren

Clinical Research Coordinator II

Detroit, MI · On-site

$24 - $32/hr

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the ...

McLaren

Clinical Research Coordinator II

Detroit, MI · On-site

$24 - $32/hr

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the ...

McLaren

Clinical Research Coordinator II

Detroit, MI · On-site

$24 - $32/hr

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the ...

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Trials Manager information

What is a trials manager?

Trials Managers are professionals responsible for overseeing and coordinating clinical trials or research studies. They manage all aspects of the trial process, including planning, organizing, and ensuring that studies are conducted in accordance with regulatory guidelines and protocols. Their role often involves liaising with sponsors, investigators, and regulatory authorities, as well as monitoring progress and reporting results. Trials Managers play a key role in ensuring that trials are completed on time, within budget, and to the required quality standards.

What are the main challenges a trials manager faces when coordinating multi-site clinical trials?

As a Trials Manager, one of the primary challenges when overseeing multi-site clinical trials is ensuring consistent protocol adherence and data quality across all locations. This involves frequent communication with site staff, troubleshooting logistical issues, and monitoring regulatory compliance. Additionally, balancing timelines and resources while managing diverse teams can be demanding. Successful Trials Managers proactively address these challenges through robust planning, regular site visits, and clear documentation to keep studies on track.

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

To thrive as a Trials Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a relevant scientific degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and often certifications like ACRP or SOCRA are highly valuable. Strong leadership, organization, and communication skills help manage multidisciplinary teams and ensure protocol adherence. These competencies are crucial for delivering safe, efficient, and compliant clinical trials that advance medical research.

What is the difference between Trials Manager vs Clinical Research Coordinator?

CriteriaTrials ManagerClinical Research Coordinator
Required CredentialsBachelor's degree, experience in trial management, knowledge of regulationsBachelor's degree, clinical research experience, regulatory knowledge
Work EnvironmentOversees multiple trials, manages teams, coordinates with sponsorsHandles daily trial activities, patient interactions, data collection
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, clinics, research institutions

The Trials Manager focuses on overseeing entire clinical trials, managing teams, and ensuring compliance across multiple studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, working directly with patients and collecting data. Both roles require similar educational backgrounds and regulatory knowledge but differ in scope and responsibilities.

What are popular job titles related to Trials Manager jobs in Michigan?

For Trials Manager jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Trials Manager jobs in Michigan look for?

The top searched job categories for Trials Manager jobs in Michigan are:

Trials Manager jobs near you
Infographic showing various Trials Manager job openings in Michigan as of August 2026, with employment types broken down into 80% Full Time, 19% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution.

Clinical Research Coordinator

Livonia, MI • On-site

Hypertension Nephrology Associates
Outpatient Health Care • 11 - 50 employees
Learn more about Hypertension Nephrology Associatesexternal

$22.75 - $30.25/hr

Other

Medical, Dental, Retirement, PTO

Re-posted 7 days ago

Job description

Position Overview

We are seeking a detail-oriented and patient-focused Clinical Research Coordinator to support our clinical research program. This role combines clinical care responsibilities with research coordination and administrative support.

The ideal candidate will bring experience in clinical trials, strong organizational skills, and a foundational understanding of study protocols and GCP guidelines. This role is well-suited for a Medical Assistant with research experience who is looking to further develop their skills in a clinical trials setting.

RESPONSIBILITIES
  • Assist in the coordination and execution of clinical trial activities in accordance with study protocols and ICH-GCP guidelines
  • Prepare study materials, equipment, and documentation for patient visits
  • Conduct protocol-specific procedures, interviews, and data collection
  • Maintain accurate and complete study documentation, including regulatory binders and source documents
  • Perform data entry and resolve study-related data queries
  • Verify patient records post-visit to ensure completeness and protocol compliance
  • Support subject recruitment, visit tracking, scheduling, and study-related financial tracking
  • Assist with the development and maintenance of source documents
  • Maintain organized and audit-ready study files (paper and electronic)
  • Provide administrative support across active clinical trials
  • Assiist providers with patient care workflows during clinic visits
  • Collect patient medical histories and document clinical information
  • Perform vital signs, phlebotomy, and basic clinical procedures
  • Support medication reconciliation and communicate updates to providers
  • Maintain accurate documentation in the Electronic Medical Record (EMR) system
  • Educate patients on treatment plans, study participation, and follow-up care
  • Assist with scheduling, patient communication, and follow-up coordination
  • Ensure a clean, organized, and well-functioning clinical environment
QUALIFICATIONS
  • Previous administration experience in a private practice or clinical setting
  • IT Proficiency (Microsoft Office package)
  • Good verbal and written communication skills
  • Strong attention to detail and organizational skills
  • Proficiency with electronic medical records (EMR) and electronic data capture (EDC) systems
  • Clinical trials and/or medical practice experience
  • Experience managing essential documents for clinical trials according to ICH GCP
  • Experience using electronic data capture systems
  • Experience with phlebotomy, EKG, and Vital signs collection
  • Associate's degree in a science, technical, health-related field, or another applicable discipline (not required in lieu of experiences and certifications
BENEFITS
  • Completion of Good Clinical Practice (GCP) training
  • CME hours
  • 401(k)
  • Dental insurance 
  • Health insurance 
  • Paid time off 
LOCAL CANDIDATES PREFERRED / NO RELOCATION ASSISTANCE / WORK SPOONSHIP WILL NOT BE PROVIDED WITH THIS ROLE
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