Clinical Research Associate Jobs in Michigan, United States

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.

Our FSP team is currently seeking experienced CRA 2s located near major hub airports across the US with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture.

Our FSP team is currently seeking a CRA 2 in West, Central, or South Regions with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' r

Headlands Research – Metro Detroit is seeking a Clinical Research Coordinator to coordinate assigned clinical trials from site initiation to study close-out at the Detroit, MI site. Day-to-day responsibilities include conducting subject visits, maintaining ALCOA-C compliant documentation, managing subject recruitment and retention, ensuring timely EDC data entry, reporting adverse events, and collaborating with investigators, lab teams, sponsors/CROs, and internal stakeholders.

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.

Headlands Research – Metro Detroit is a leading clinical research site in the Detroit metro area dedicated to advancing medical innovation and expanding access to clinical trials. As a Clinical Research Coordinator, you will coordinate all aspects of assigned clinical trials from site initiation to study close-out, conduct subject visits, manage recruitment and consent, ensure timely data entry, and report adverse events while collaborating with investigators, sponsors, and internal stakeholders

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.

The Clinical Research Coordinator II ensures quality research is conducted at assigned investigative sites in Bay City, Michigan, in accordance with sponsor protocols, FDA Regulations, and ICH/GCP guidelines. Day-to-day duties include conducting study subject visits, completing data entry and query resolution, overseeing adverse event reporting, and liaising with laboratory, data, and administrative teams to meet enrollment goals.

Iterative Health is a healthcare technology and services company accelerating clinical research across gastrointestinal, hepatology, obesity, and cardiology. As a Clinical Research Coordinator II in Troy, Michigan, you will independently coordinate daily study activities for industry-sponsored clinical trials from start-up through closeout with minimal supervision.

DM Clinical Research coordinates investigational product dispensing for clinical trials, ensuring compliance with study protocols and blinding plans. The Coordinator compounds and dispenses IP, manages inventory, conducts audits, and trains new team members.

Headlands Research, a network of advanced clinical trial sites, advances medicine by delivering high-quality, patient‑centered clinical research. The Site Manager/Director leads operational leadership and study management at the Grand Rapids site, overseeing facilities, CTMS, regulatory compliance, financial performance, and team development.

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.

Headlands Research Clinical Research team supports clinical trial delivery across community sites, leveraging technology and support services to expand patient participation. Clinical Research Assistants help execute trials by assisting with study visits, preparing materials, collecting and organizing data, and ensuring protocol compliance while interacting directly with patients and care teams.

Sponsored Programs Cancer and Specialty Health Research Operations at Corewell Health seeks a Registered Nurse Clinical Research specialist focused on pediatric oncology. The role coordinates protocols, recruits participants, manages regulatory documentation, and ensures compliance with FDA, NIH, and HIPAA standards.

Nursing Solutions Group at Science 37 delivers mobile clinical nurse services for decentralized clinical trials. The Per Diem Clinical Research Nurse provides patient care at participants' homes, collaborates with study teams, and supports trial implementation across multiple therapeutic areas.