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Clinical Research Operations Manager Jobs in Michigan

Actalent

Research Educator

Detroit, MI

Clinical Research QA Education Project Manager This role sits within the Quality team supporting ... Strong understanding of clinical research operations, including protocol review, execution ...

Insight

Research Executive Assistant

Flint, MI · On-site

$18.75 - $25.75/hr

... operational, and project coordination support to Insight Health System's Clinical Research ... Key Responsibilities: • Manage complex calendars, meeting coordination, and travel arrangements ...

Insight

Research Executive Assistant

Flint, MI

$18.75 - $25.75/hr

... operational, and project coordination support to Insight Health System's Clinical Research ... Key Responsibilities: • Manage complex calendars, meeting coordination, and travel arrangements ...

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Clinical Research Operations Manager information

See Michigan salary details

$30.5K

$85.5K

$162.6K

How much do clinical research operations manager jobs pay per year?

As of Aug 4, 2026, the average yearly pay for clinical research operations manager in Michigan is $85,450.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,200.00 and $98,900.00 per year, depending on experience, location, and employer.

How does a clinical research operations manager collaborate with cross-functional teams during a study?

As a Clinical Research Operations Manager, you will work closely with cross-functional teams including clinical trial coordinators, data managers, regulatory affairs specialists, and principal investigators. Your role involves facilitating clear communication between departments, ensuring that study milestones are met, and resolving operational issues as they arise. Regular meetings and status updates are common, and you'll often act as a liaison to keep all stakeholders aligned on study objectives, timelines, and compliance requirements. This collaborative approach is crucial for maintaining study integrity and ensuring successful trial outcomes.

What does a clinical research operations manager do?

A Clinical Research Operations Manager oversees the daily operations of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. They coordinate between research staff, sponsors, and regulatory bodies, manage budgets and timelines, and ensure proper documentation and reporting. Their role is essential in maintaining the quality and integrity of clinical studies from start to finish.

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

To thrive as a Clinical Research Operations Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications such as ACRP or SOCRA are highly valuable. Leadership, problem-solving, and excellent organizational and communication skills help you manage teams and collaborate effectively with stakeholders. These skills and qualities are crucial for ensuring the successful execution of clinical trials while maintaining regulatory standards and operational efficiency.
What are popular job titles related to Clinical Research Operations Manager jobs in Michigan? For Clinical Research Operations Manager jobs in Michigan, the most frequently searched job titles are:
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Clinical Research Operations Manager jobs near you
Infographic showing various Clinical Research Operations Manager job openings in Michigan as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $85,450 per year, or $41.1 per hour.

Associate Director Research Operations

Insight

Flint, MI • On-site

Full-time

Posted 11 days ago

Job description

Insight Health System Clinical Research
JOB DESCRIPTION
Associate Director, Research Operations
Title: Associate Director - Research Operations
Location: Michigan
Reports To: Director of Research Operations
Schedule: Full-time, with flexibility for study visits, sponsor meetings, and operational needs
Position Summary:
The Associate Director of Research Operations is responsible for supporting Insight Health System's clinical research enterprise across multiple sites. This role is 50% focused on clinical Trials operations oversight and 50% dedicated to central feasibility, start up, regulatory, contracts and budgets, and quality functions. The Associate Director ensures operational excellence, compliance, and efficient execution of research activities across the network.
Key Responsibilities:
Clinical Operations Leadership (50%):
• Oversee day-to-day clinical research operations across assigned regions/sites
• Support site managers, team leads, coordinators, assistants, and investigators to ensure protocol adherence and visit execution
• Monitor enrollment performance, visit scheduling, and resource allocation
• Troubleshoot operational barriers and implement workflow improvements
• Support onboarding, training, and competency development for research staff
• Capability of travel between multiple locations as needed to support operational activities
Feasibility, Regulatory, Contracts, Budgets, and Quality (50%):
• Collaborate with Feasibility and start up/regulatory teams to ensure timely FQ submissions, IRB submissions, amendments, and reporting
• Support contract and budget negotiations, including feasibility review and cost analysis
• Ensure quality standards across documentation, data entry, and essential files
• Participate in internal audits, monitoring visits, and CAPA development
• Maintain alignment with SOPs, GCP, IRB and institutional requirements
  • Review study protocols and develop source
  • Maintain ISF documentation

Cross-Functional Collaboration:
• Serve as a liaison between research operations, regulatory, finance, legal, and executive leadership
• Support strategic planning for site growth, service expansion, and operational scaling
• Contribute to SOP development, process optimization, and system implementation
Minimum Qualifications:
• Ph.d degree in life sciences, healthcare, or related field (required)
• 5-7 years of clinical research experience, including operational leadership
• Strong knowledge of GCP, FDA regulations, IRB processes, and site management
• Experience with budgets, contracts, and regulatory and quality workflows
• Excellent communication, leadership, and problem-solving skills

Apply