Clinical Research Associate Jobs in Ohio, United States

IQVIA’s Clinical Research team builds and monitors clinical trials to accelerate medical innovation. The Clinical Research Associate conducts site monitoring visits, manages regulatory submissions, and ensures protocol compliance across multiple study sites.

Senior Clinical Research Associate with 2+ years on‑site monitoring experience. Conduct site monitoring, recruitment tracking, protocol training, and regulatory submissions.

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.

Fortrea's FSP team is seeking a Clinical Research Associate 2 to deliver high-standard clinical trial monitoring across Ohio, Pennsylvania, or Virginia. Day-to-day, you will manage all aspects of site monitoring (routine and close-out), conduct pre-study and initiation visits, verify informed consent and protocol adherence, review CRFs and resolve queries, handle SAE reporting, and support registry management and feasibility work.

Merck seeks a Senior Clinical Research Associate to manage ophthalmology clinical trials across the US. The role ensures site compliance with ICH/GCP standards, monitors study conduct, and mentors junior staff while maintaining strong investigator relationships. This is a fully remote position requiring residence in specific states.

Merck seeks a Senior Clinical Research Associate to manage ophthalmology clinical trials across multiple US states. The role involves site monitoring, compliance oversight, and mentorship while operating remotely with significant travel.

Clinical Operations at Worldwide Clinical Trials drives clinical research across therapeutic areas. The Senior Clinical Research Associate, CNS/Psychiatry, Midwest manages site activities, conducts study initiation visits, and ensures regulatory compliance remotely while traveling regionally as needed.

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.

The Research Associate in the RI Clinical & Translational (Kerlin) unit at Main Campus, Columbus, OH conducts independent research alongside a Principal Investigator, managing basic and complex projects to meet timelines, deliverables, and expectations. Day-to-day work includes designing and running laboratory experiments, collecting and statistically analyzing data, maintaining accurate records, preparing reports and presentations, mentoring junior staff, and assisting with scientific publicati

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.

FSP team at Covance seeks Senior Clinical Research Associate 2 to lead monitoring of in‑vitro diagnostics trials across the US. The role conducts site monitoring, data verification, SAE reporting and supports site staff training while ensuring protocol compliance. Remote work from any US location with 50‑60% overnight travel required.

Clinical Trials Management Office at The Ohio State University coordinates IBD clinical research studies within the Gastro/Hepatology/Nutrition Division. The Clinical Research Coordinator manages patient recruitment, consent, scheduling, sample collection, adverse event monitoring, and regulatory compliance while supporting data analysis and reporting.

The Clinical Research-RN role at MOB Lindner Research supports clinical trial start-up and execution in acute care, inpatient, and outpatient settings. Day-to-day duties include educating physicians and hospital staff, implementing study protocols, facilitating patient enrollment and follow-up, ensuring protocol compliance, reporting to sponsors, and coordinating with patients' clinical health plans.

The Clinical Research Medical Assistant (CRMA) supports the Clinical Research department at MOB Lindner Research HV in Ohio, United States. The role facilitates and coordinates daily clinical trial activities, ensuring efficient participant flow through the department.

Heart & Vascular Research Clinical Services at OhioHealth coordinates clinical studies to advance cardiovascular science. The Clinical Research Coordinator partners with the Principal Investigator to recruit and screen participants, obtain consent, collect and enter data, and ensure compliance with GCP and federal regulations.

Manager Clinical Research leads the TriHealth Hatton Research Institute’s clinical research program, overseeing planning, organization, and compliance with FDA, HHS, USDA, and AAALAC regulations. The role drives strategic initiatives, manages a multidisciplinary team, and ensures high-quality, compliant clinical trials.

Hatton Research Institute (TriHealth) focuses on advancing clinical research to improve patient outcomes. As a Clinical Research Nurse, you coordinate study protocols, screen and enroll participants, and ensure compliance with IRB/FDA standards while collaborating with investigators and hospital staff.

Radiology Department, Medicine at The Ohio State University supports clinical research studies. The Clinical Research Assistant helps implement and coordinate studies, recruits participants, conducts behavioral or diagnostic testing, and manages data collection and reporting.

The Clinical Research Coordinator-Float at The Ohio State University supports the College of Medicine’s clinical trials by coordinating daily research activities, recruiting and enrolling patients, obtaining informed consent, and ensuring compliance with regulatory and sponsor requirements. The role involves assessing patient eligibility, scheduling appointments, collecting and processing biological samples, monitoring for adverse events, and maintaining accurate data records.

Care Access Clinical Research team advances health equity by conducting community‑focused clinical studies. The Clinical Research Coordinator II screens, enrolls and monitors study participants, ensures protocol and regulatory compliance, manages site logistics and documentation, and coordinates with investigators and sponsors.