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.

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.

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

BASIC SUMMARY: Performs QC and coordinates all study-related activities of technical staff to ensure compliance with the protocol and applicable SOPs and maintains the raw data for nonclinical studies.

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.

The Clinical Research Associate (CRA) is a primary point of contact at the site level for both internal and external stakeholders, responsible for overseeing the quality, integrity and compliance of clinical trial sites in accordance with the protocol, Standard Operating Procedures (SOPs), International Council for Harmonization (ICH) Guideline for Good Clinical Practice (GCP), and applicable regulatory requirements.

To be eligible for this position, you must reside in the same country where the job is located. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance. Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials.

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5+ years of monitoring residing in the Midwest area.

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.

Our FSP team is currently seeking Ophthalmology Sr. CRAs with 4+ years of monitoring residing on the East Coast of the US.

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

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 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.

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.

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.

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.

TriHealth Hatton Research Institute coordinates Phase II‑IV clinical trials, ensuring safety, integrity, and high‑quality patient care. The Clinical Research Coordinator manages protocol execution, regulatory compliance, and subject assessments while collaborating with multidisciplinary teams.

This part‑time RN position supports inpatient clinical research studies at Cincinnati Children’s Hospital. The role involves day shifts, flexible scheduling, and up to 40 hours per week, with pay of $38 per hour.