Clinical Research Associate Jobs in Michigan, United States

<p style="text-align:left"><b>Job Description</b></p><p style="text-align:inherit"></p><p><b><u>CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS</u>: ALABAMA, GEORGIA, COLORADO, MASSACHUSETTS, MICHIGAN, MARYLAND, PENNSYLVANIA</b></p><p></p><p>The role is accountable for performance and compliance for assigned protocols and sites in a country.</p><p></p><p>Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company

Revival Research Institute seeks a Physician Assistant to support clinical trials in Southfield, MI. The role involves conducting participant assessments, ensuring protocol compliance, and managing safety surveillance under Principal Investigator oversight. This is a full-time, on-site position focused on maintaining data integrity and regulatory adherence.

Clinical Research team at Merck conducts oncology trials across the US. The Clinical Research Associate manages site relationships, ensures protocol compliance, performs remote and on‑site monitoring, and collaborates with cross‑functional groups to drive study performance. Remote work, candidates must reside in listed states, travel 65‑75% of time, 2‑3 days/week on site.

AbCellera is a clinical-stage biotechnology company developing antibody-based medicines across endocrinology, women's health, immunology, and oncology. The Senior Clinical Research Associate serves as the primary link between AbCellera and investigative sites, owning a portfolio of complex sites and executing the full monitoring lifecycle from site selection through close-out.

Clinical Operations at Worldwide Clinical Trials drives multi‑therapeutic clinical studies, including oncology, by managing site activities and ensuring regulatory compliance. The Senior Clinical Research Associate oversees site start‑up, monitoring, data collection, safety reporting, and study close‑out, primarily remotely while coordinating with sites across the Northeast and Midwest.

Fortrea's FSP team is seeking a Clinical Research Associate 2 for the Central Region to deliver high-standard clinical trial monitoring and participant care across a remote territory spanning multiple states. Day-to-day, the role covers full-cycle site monitoring, pre-study and initiation visits, CRF review and query resolution, SAE reporting, and registry management, with 8-10 on-site days per month.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate, Oncology, manages site activities from start-up to closeout, conducts initiation visits, ensures regulatory compliance, and supports safety reporting.

Fortrea's FSP team is hiring experienced Clinical Research Associates (CRAs) specializing in Ophthalmology monitoring across major US hub locations. The role involves full-cycle study site monitoring, CRF review, SAE reporting, and ensuring participant safety and data integrity in a fast-paced, technology-driven clinical research environment.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate manages site activities for CNS and rare disease studies, conducts initiation visits, ensures regulatory compliance, and supports data collection remotely.

AbCellera, a clinical-stage biotechnology company focused on antibody-based drug discovery, is seeking a Senior Clinical Research Associate to serve as the primary liaison between the company and its investigative sites. Day-to-day, you will oversee multiple complex sites from selection through initiation, routine monitoring, and close-out, ensuring regulatory compliance, data integrity, and operational excellence while protecting patient safety.

Fortrea’s Monitoring Excellence Academy is hiring Clinical Research Associates (CRA 1) for Oncology, CAR T, or Ophthalmology trials. The role involves site monitoring, data integrity verification, SAE reporting, and supporting study site operations across Central or West coast US hubs or Montreal, Canada.

Corewell Health’s Sponsored Programs Heart and Vascular Institute Research Operations seeks a Clinical Research Specialist in Grand Rapids, MI. This hybrid role supports principal investigators by coordinating research studies, managing project logistics, and ensuring regulatory compliance. The specialist handles subject recruitment, data collection, and adverse event monitoring while collaborating with sponsors and multidisciplinary teams.

Sponsored Programs Cardiovascular team at Corewell Health conducts clinical research to advance cardiovascular treatments. The Registered Nurse Clinical Research coordinates protocols, recruits and enrolls participants, manages regulatory documentation, and ensures compliance with FDA, NIH, and HIPAA standards.

The RN Clinical Research Neurology role within the Sponsored Programs Neurosciences and Behavioral Health Research Operations department at Corewell Health's Secchia Center in Grand Rapids, MI, supports principal investigators by preparing, evaluating, and implementing clinical research studies to advance clinical practice. Day-to-day, the coordinator/project manager handles operational feasibility, budget development, IRB documentation, protocol operations, subject recruitment and enrollment, d

Michigan Institute of Urology seeks a Clinical Research Navigator, RN to join its clinical trials team in Troy, MI. This role bridges research and patient care by overseeing trial execution, including participant recruitment, data entry in EDC systems, and direct nursing coordination. The position operates on a full-time, Monday–Friday day shift schedule.

Sponsored Programs Oncology West at Corewell Health conducts oncology clinical research to advance patient care. The RN coordinates and manages research studies, prepares IRB documents, develops budgets, and ensures protocol operations under principal investigator oversight.

Sponsored Programs Heart and Vascular Institute Research Operations at Corewell Health conducts clinical research to advance structural heart care. The Registered Nurse Clinical Research Structural Heart coordinates and manages studies, prepares IRB documents, enrolls patients, and ensures regulatory compliance while collaborating with investigators and multidisciplinary teams.

The Clinical Research Specialist 1 at Corewell Health's Sponsored Programs Bio Bank in Grand Rapids, MI, prepares, evaluates, and implements clinical research studies under principal investigator oversight to advance clinical practice. Day-to-day, the role coordinates and manages studies of low to moderate complexity, handling IRB documentation, protocol operations, subject recruitment and screening, data collection, and compliance with GCP and regulatory requirements.