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Trials Manager Jobs in Michigan (NOW HIRING)

Manage assigned protocols and activities. * Knows the EPIC EMR system to coordinate patient care in ... and clinical trials. * Experience with computer data entry and database management * Excellence ...

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 ...

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 ...

Manage assigned protocols and activities. * Knows the EPIC EMR system to coordinate patient care in ... clinical trials. • Experience with computer data entry and database management • Excellence ...

Updates the Clinical Trials Management System (CTMS). * Responsible for obtaining required signatures on clinical trial documents and returning within specified time frames. * Candidate will receive ...

Portfolio Manager

Ann Arbor, MI · On-site

$89K - $111K/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 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.

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 Trials Research Coordinator

Grand Rapids, MI • On-site

$60 - $80/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago


Job description

Join BAMF Health, where you're not just part of a team; you're at the forefront of a revolution in Theranostics, changing lives for the better. As a member of our global team, you'll contribute to pioneering technology and deliver top-tier patient care. Located in the heart of downtown Grand Rapids, our cutting‑edge global headquarters resides within the state‑of‑the‑art Doug Meijer Medical Innovation Building. Step into our modern and spacious facilities, where innovation thrives and collaboration knows no bounds. Join us in our mission to make Theranostics accessible and affordable for all, and be part of something truly remarkable at BAMF Health. The Clinical Research Coordinator (CRC) plays a pivotal role in conducting clinical trials focused on investigational PET tracer and radiopharmaceutical therapies. Works closely with a team of medical professionals and researchers to ensure our clinical trials are conducted efficiently, ethically, and within regulatory compliance. Responsible for managing all aspects of the clinical trials, from participant recruitment to data collection and analysis, ensuring the integrity and quality of the research.

Duties and Responsibilities
  • Coordinate and manage clinical trials from initiation to closure, including patient recruitment, screening, enrollment, and follow-up.
  • Patient recruitment.
  • Pre-screen potential candidates medical records for appropriateness for participation.
  • Coordinate all necessary resources for successful conduct of clinical trial protocol, including: providers, clinic rooms, clinic staff, imaging equipment, radiopharmacy, etc.
  • Maintain accurate and complete clinical trial documentation and records.
  • Facilitate communication between the clinical site, research team, and sponsors.
  • Train and oversee research staff and volunteers, as necessary.
  • Manage the procurement, storage, and handling of study materials, including investigational products and radiopharmaceuticals.
  • Ensure participant safety and confidentiality according to HIPAA regulations.
Basic Qualifications
  • Bachelor's degree in a life sciences field, nursing, or a related area or equivalent required
  • 1 year of experience in human subjects research required
  • BLS within 30 days of hire required
  • Shipping and Handling of Specimen Training - Certification within 30 Days of hire required
  • GCP Certification within 30 Days of hire required
Preferred Qualifications
  • Advanced educational degree preferred.
  • 3 years of experience in healthcare, direct patient care preferred.
  • Understanding of Good Clinical Practice (GCP), FDA regulations, and IRB requirements required.
  • Experience in oncology, radiology, or a related field preferred.
  • Familiarity with PET imaging, radiopharmaceuticals, and the unique considerations of trials involving these modalities preferred.
  • Shipping and Handling of Specimen Training - Certification within 30 Days of hire required.
  • SOCRA Certified Clinical Research Professional (CCRP) or ACRP Certified Professional (ACRP-CP) or ACRP Certified Clinical Research Coordinator (CCRC) - preferred.
Schedule Details
  • Employment Status: Full time (1.0 FTE)
  • Weekly Scheduled Hours: 40
  • Hours of work: 8:00 a.m. and 4:30 p.m.
  • Days worked: Monday-Friday with some flexibility.
  • A hybrid work opportunity is available after the introductory period, with the option to work remotely 1 day per week.

At BAMF Health, our top priority is patient care. To ensure we are able to drive a Bold Advance Medical Future, we offer a well‑rounded benefit package to care for our team members and their families.

Benefits
  • Employer paid High Deductible Health Plan with employer HSA contribution
  • Flexible Vacation Time
  • 401(k) Retirement Plan with generous employer match
  • Several benefit options including, but not limited to
  • dental
  • vision
  • disability
  • life
  • supplemental coverages
  • legal and identity protection

Disclaimer BAMF Health provides equal opportunities to all employees for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

BAMF Health will reasonably accommodate qualified individuals with a disability so that they can perform the essential functions of a job unless doing so causes a direct threat to these individuals or others in the workplace and the threat cannot be eliminated by reasonable accommodation or if the accommodation creates an undue hardship to BAMF Health.

BAMF Health is an Equal Opportunity Employer and will not accept or tolerate discrimination or harassment against any applicant, employee, intern, or volunteer based upon the following characteristics: race, color, religion, creed, national origin, ancestry, sex, age, qualified mental or physical disability or handicap, sexual orientation, gender identity/expression, transgender status, genetic information, pregnancy or pregnancy‑related status, marital status, veteran status, military service, any application for any military service, or any other category or class protected by applicable federal, state, or local laws.

BAMF Health is creating a Bold Advanced Medical Future by developing a network of advanced cyclotron equipped Radiopharmacies and Theranostics centers.

Powered by our proprietary AI platform, our clinics deliver personalized treatment to patients with cancer and neurodegenerative diseases.

At BAMF Health, we are committed to creating a diverse, inclusive, and equal opportunity workplace.

BAMF Health’s Clinicians, Researchers, Radiopharmacy, Engineering, Technology, and Operations experts have designed, planned, and built the world’s most advanced platform for Theranostics at our global headquarters in Grand Rapids, Michigan.

The world‑leading Theranostics Center includes the world’s most advanced dual‑cyclotron equipped Radiopharmacy, Molecular Imaging Clinic with Total Body PET/CT and PET/MR scanning capabilities, and molecular therapy clinic with advanced SPECT/CT application.

BAMF’s world‑class healthcare facility is leading the health care industry towards a Bold Advanced Medical Future, where patients are empowered to regain their quality of life.

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