Clinical Research Associate Jobs in Michigan, United States

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.

FSP Clinical Research Team conducts oncology trials to advance cancer therapies. The CRA monitors study sites, conducts pre‑study and initiation visits, ensures protocol compliance, reviews CRFs, reports serious adverse events, and supports site staff.

Clinical Research Associate II on the PPD Development team at Thermo Fisher Scientific, driving clinical monitoring and site management for oncology and ophthalmology trials. The role conducts remote and on‑site visits, applies risk‑based monitoring, ensures protocol compliance, and collaborates with investigators to maintain audit readiness.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas, including rare CNS diseases. The Senior Clinical Research Associate manages site activities from start-up through closeout, conducts initiation visits, ensures regulatory compliance, and supports regional travel while primarily working remotely.

Worldwide Clinical Trials seeks a Senior Clinical Research Associate to manage site research activities for non-interventional studies across cardiovascular, metabolic, neuroscience, oncology, and rare diseases. Responsibilities include site selection, regulatory documentation, contract negotiation, training, monitoring, and study closure.

Senior Clinical Research Associate at ProPharma Group responsible for monitoring clinical sites, conducting site initiation, interim, and close-out visits, and ensuring compliance with SOPs and regulatory requirements. Duties include monitoring report writing, site personnel training, data review, and investigational supply management.

ProPharma Group, with 20 years of experience, enhances patient health by partnering with biotech, medical device, and pharmaceutical companies. Through an advise‑build‑operate model, the firm delivers end‑to‑end regulatory science, clinical research, quality & compliance, pharmacovigilance, medical information, and R&D technology solutions.

Academic Research Project at Trinity Health focuses on clinical research in obstetrical care. The associate coordinates daily study activities, recruits patients, obtains consent, conducts surveys, manages data, and supports IRB reporting under senior staff guidance.

Associate Counsel manages full lifecycle of clinical trial agreements, drafting, reviewing, negotiating contracts and budgets for industry-funded studies. Provides legal services to Trinity Health System Office and Ministries, advising senior management, coordinating outside counsel, ensuring compliance with institutional policies and regulations.

Academic Research Project at Trinity Health Ann Arbor focuses on obstetrical clinical studies. The role coordinates day‑to‑day research activities, screens patients, obtains informed consent, collects and cleans data, and supports IRB reporting.

The Associate Director, Clinical Sciences, Internal Medicine leads the development, evaluation, planning, and execution of internal medicine clinical studies, ensuring scientific integrity and interpretation of study data. Working in a matrixed, cross‑functional team with internal and external vendors, the role may serve as a Clinical Scientist or delegate, contribute to program meetings, scientific advisory boards, steering committees, and data/safety monitoring.

We are seeking a detail-oriented Research Assistant to support clinical trial activities in compliance with regulations. The role involves EDC entry, query resolution, regulatory binder maintenance, scheduling subject visits, building relationships with study team, recruiting and enrolling subjects, coordinating follow-up care, ensuring adherence to IRB protocols, supporting subject safety, and complying with SOPs.

LabCorp seeks a Sample Collection Technician to support nonclinical and clinical research studies in Madison, WI. The role focuses on blood and biological sample collection, documentation, and data management while ensuring compliance with SOPs, GLPs, and regulatory guidelines. Responsibilities include sample processing, record keeping, animal health monitoring, data entry, study coordination, and client support.

Medical Assistant – Certified Nursing Assistant – Pharm Tech role at Profound Research supports clinical trial operations in Detroit. The assistant coordinates patient recruitment, data collection, and regulatory compliance under site management and PI guidance.

Job Summary The IRB Associate will support the activities and operations of the Corewell Health Office of the IRB within the Corewell Health Research Institute (CHRI). The IRB Associate will assist IRB staff with the daily operational tasks required to review and approve submissions to the IRB, conduct IRB Committee meetings, and maintain office records.

Grand Valley State University seeks an Assistant or Associate Professor in Nursing to join the Kirkhof College of Nursing at its Health Campus in Grand Rapids, MI. The role blends teaching, scholarship, and service, with opportunities for professional practice and interdisciplinary collaboration. Candidates will integrate the KCON philosophy into classroom and clinical instruction, maintain current knowledge through scholarly activities, and apply learning to both academic and clinical settings.

Grand Valley State University seeks an Associate Professor and Doctor of Physical Therapy Program Director to lead its accredited DPT program. The role combines academic leadership, curriculum oversight, and faculty development within a 12‑month tenure‑stream position.

At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them.

Associated Retinal Consultants, a nationally recognized retina specialty practice, seeks a BC/BE fellowship-trained Vitreoretinal Surgeon to join its team in Traverse City, Michigan. The role offers a collaborative environment focused on clinical excellence, research participation, and cutting‑edge patient care within a leading eye‑care network.