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Trials Manager Jobs in Michigan (NOW HIRING)

Actalent

Clinical Research Coordinator

Detroit, MI

$24 - $31.75/hr

Support all active studies within the assigned hematology team rather than owning a single study, contributing to consistent coverage across multiple trials. * Manage a patient load of approximately ...

CTI

Project Manager, Laboratory Services

Milan, MI · On-site

Expected to manage medium to high complexity trials. * Set goals and timelines, provide oversight and foster motivation within the team to accomplish goals within defined timelines and with high ...

Actalent

Project Manager

Detroit, MI

Project Manager - Clinical Research Training and Quality The Project Manager will serve as a key ... Lead education and training initiatives for the Quality team supporting cancer, clinical trials ...

University of Michigan

Portfolio Manager

Ann Arbor, MI · On-site

$89K - $110K/yr

You will help to lead the project management team in addition to managing your own clinical trials. You will report to the SABER Assistant Director of Project Management and Quality. You may be asked ...

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Trials Manager information

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 are Trials Managers?

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 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 July 2026, with employment types broken down into 83% Full Time, 15% Part Time, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.
Associate Director of Clinical Trials Unit/Associate Professor Position

Associate Director of Clinical Trials Unit/Associate Professor Position

University of Michigan

Ann Arbor, MI • On-site

Full-time

Posted 14 days ago

University Of Michigan rating

8.1

Company rating: 8.1 out of 10

Based on 144 frontline employees who took The Breakroom Quiz

152nd of 611 rated colleges and universities

Job description

Description
The Department of Biostatistics at the University of Michigan is seeking an experienced biostatistician to help lead the Statistical Analysis of Biomedical and Educational Research (SABER) group as Associate Director. Begun in 1999, SABER is the data coordinating center (DCC) for several NIH-funded networks and multicenter trials and cohort studies. The areas of application include pulmonology, diabetes, cardiovascular disease, neurology, rheumatology, and emergency medicine. The current staff of 38 includes statisticians, database administrators, data managers, software developers, project managers, clinical monitors and research administrators.
The Associate Director will be appointed as a senior faculty member in the Department of Biostatistics at the Associate or Full Professor level in research track. Rank will be commensurate with experience. Applicants must have a Ph.D. or equivalent degree. The Associate Director will work closely with the SABER Director to effectively run the SABER unit by streamlining operations and budgets and implementing new ideas. The Associate Director will collaborate with clinician-scientists to identify ideas for sponsored research, and on the submission of applications for their funding. Generous salary and start-up support are available.
The Department of Biostatistics has 43 primary faculty members and 230 full-time PhD and Master's students. The Department is involved in cutting edge methodological research and scientific investigation in many areas of public health and biomedical research. The Department has close ties with the Department of Statistics, the Institute for Social Research, the Medical School, the Michigan Institute for Data Science, The Institute of Health Policy and Innovation, the University of Michigan Rogel Cancer Center, and other research groups across campus. Approximately 80% of SABER's portfolio is in collaboration with University of Michigan Medical School faculty.
The University of Michigan offers competitive salaries and excellent benefits. Ann Arbor is a progressive city of about 120,000 year-round residents, and approximately 44,000 students, with excellent schools and a wide variety of sporting and musical activities. It is rated very highly in national surveys for its quality of life and has the amenities of a city many times its size.
The University of Michigan is an affirmative action/equal opportunity employer. Applications from women and minorities are welcomed and strongly encouraged.
Qualifications
Candidates must have substantial experience designing and leading large, multicenter clinical research network projects, involving clinical trials, cohort studies, or registries. They must have experience working in cross-functional study teams, including those functions necessary for successful and innovative data coordinating centers, such as data management systems and operations, reporting for data monitoring committees, clinical research coordination and clinical monitoring, and quality control procedures. They should have a track record of research in an area related to clinical trials or cohort studies, such as adaptive designs, methods for missing data, analytical procedures for causal inference, and statistical monitoring approaches. In addition, successful candidates should have excellent communication skills and administrative acumen, and the ability to work effectively in a clinical and academic environment.
Underfill Statement: The rank of the selected candidate will depend upon the candidate's qualifications. For more information regarding appointment criteria for these job titles, please visit https://research.umich.edu/appointments-promotions#9.
Application Instructions
Consideration of applications will begin on a rolling basis. Interested applicants should submit their CV, a statement of research interest, the names of three references, and academic transcripts (if a recent graduate).

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About University of Michigan

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The University of Michigan (U-M), based in Ann Arbor, MI, US, is one of America's most esteemed institutions in higher education. Established in 1817, it presides in the industry of education and research, providing a range of services including undergraduate, graduate, and professional education programs. Complementing this is an extensive research activity that has significantly contributed to various fields, from healthcare to engineering, humanities to sports. Upholding its mission "to serve the people of Michigan and the world through preeminence in creating, communicating, preserving and applying knowledge, art, and academic values", U-M consistently ranks among the top universities globally, a testament to its tradition of excellence in learning and research, and a deep commitment to innovation and discovery.

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Headquarters location

Ann Arbor, MI, US

Year founded

1817

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