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Clinical Research Manager Jobs in Rochester, MI (NOW HIRING)

McLaren

Clinical Research Coordinator II

Detroit, MI · On-site

$24 - $32/hr

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials ... research certification preferred. Equal Opportunity Employer of Minorities/Females/Disabled ...

Spectrum Health

Research Scientist

Royal Oak, MI · On-site

... clinical research experience. Research Scientist - Health Economist requires a PhD degree in economics, health economics, health management and/or policy, health services research or related fields.

Corewell Health

Research Scientist

Royal Oak, MI · On-site

... clinical research experience. Research Scientist - Health Economist requires a PhD degree in economics, health economics, health management and/or policy, health services research or related fields.

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All JobsClinical Research JobsClinical Research Manager JobsClinical Research Manager Jobs in Rochester, MI

Clinical Research Manager information

See Rochester, MI salary details

$45.1K

$98.8K

$174K

How much do clinical research manager jobs pay per year?

As of Sep 7, 2026, the average yearly pay for clinical research manager in Rochester, MI is $98,798.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,600.00 and $112,800.00 per year, depending on experience, location, and employer.

What does a clinical research manager do?

A clinical research manager oversees clinical trials, which involve testing new medications or medical devices. Their responsibilities include ensuring all ethical practices and legal protocols are followed and that all paperwork is filled out completely and accurately. They also maintain standards for the data collection and procedures during the clinical trial and make sure all team members, including the doctors and nurses on the trial, are kept informed.

What are the key skills and qualifications needed to thrive as a clinical research manager?

To thrive as a Clinical Research Manager, you need a solid understanding of clinical trial protocols, regulatory requirements (such as GCP), and a background in life sciences or healthcare, often supported by a relevant degree. Familiarity with clinical trial management systems (CTMS), EDC software, and certifications like ACRP or SOCRA are typically expected. Strong leadership, excellent organizational skills, and effective communication abilities set outstanding managers apart. These competencies are critical for ensuring compliance, data integrity, and the successful coordination of multidisciplinary research teams.

What are some common challenges clinical research managers face when overseeing multiple clinical trials simultaneously?

Clinical Research Managers often encounter challenges such as balancing competing timelines, ensuring regulatory compliance across different studies, and effectively allocating resources among projects. Managing communication between diverse teams—such as investigators, sponsors, and regulatory bodies—can also be demanding, especially when trials are at different stages. Developing strong organizational skills and leveraging project management tools are key to successfully navigating these complexities and maintaining high standards for data quality and participant safety.

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

AspectClinical Research ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with experience in project managementBachelor's in health sciences or related field, often with certification like CCRP
Work EnvironmentOversees multiple studies, manages teams, and ensures compliance at a higher levelAssists with daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites

The Clinical Research Manager focuses on overseeing entire studies and managing teams, while the Clinical Research Coordinator handles daily study tasks and participant interactions. Both roles require relevant certifications and are essential in clinical research settings, but they differ in scope and responsibilities.

More about Clinical Research Manager jobs

What are the most commonly searched types of Clinical Research jobs in Rochester, MI?

The most popular types of Clinical Research jobs in Rochester, MI are:

What job categories do people searching Clinical Research Manager jobs in Rochester, MI look for?

The top searched job categories for Clinical Research Manager jobs in Rochester, MI are:

What cities near Rochester, MI are hiring for Clinical Research Manager jobs?

Cities near Rochester, MI with the most Clinical Research Manager job openings:

Clinical Research Manager jobs near you
Infographic showing various Clinical Research Manager job openings in Rochester, MI as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $98,798 per year, or $47.5 per hour.

Clinical Research Coordinator II

McLaren Health Care Corporation

Detroit, MI • On-site

$24 - $32/hr

Full-time

Re-posted 27 days ago

McLaren Health Care rating

6.7

Company rating: 6.7 out of 10

Based on 221 frontline employees who took The Breakroom Quiz

534th of 898 rated healthcare providers

Job description

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 clinical trials arena.
Responsibilities:
  • Assure all study requirements are met and documented and meet both internal and external regulations in accordance with protocol guidelines.
  • Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs.
  • Design systems for coordinating, compiling and submission of data; design workflow processes and participate in quality assurance measures; coordinate site visits.
  • Manage all patient and/or protocol data as assigned and respond to queries in a timely fashion.
  • Schedule and participate in monitoring visits and participate in multidisciplinary team program meetings as required.

• Bachelor's degree required or equivalent combination of education and experience.
• Medical and/or science experience/education preferred.
• Clinical research certification preferred.
Equal Opportunity Employer of Minorities/Females/Disabled/Veterans

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