Clinical Research Associate Jobs in Ohio, United States

LIFT Lab and Learning Health Systems (LHS) Collaborative team at The Ohio State University. The Clinical Research Associate Coordinator will coordinate and execute clinical research activities, manage participant recruitment, enrollment, consent, and ensure regulatory compliance.

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.

Clinical Research Associate at Ortho-Clinical Diagnostics, Inc. in Athens, OH. The role writes clinical protocols for beta-site and formal studies, sets up and monitors IVD trials, ensures data accuracy, site compliance, and manages trial master files. Onsite work in a lab/warehouse environment with flexible hours.

Precision Medicine Group's Clinical Research team drives oncology and rare disease trials with a focus on precision medicine. The Clinical Research Associate II monitors study progress, coordinates site setup, conducts visits, and ensures compliance with protocols and regulations.

Premier Research seeks a Clinical Research Associate II for the NorthEast Dermatology region to join its Global Clinical Monitoring and Site Management team. The role involves monitoring Phase I‑IV clinical trials, ensuring data integrity and patient safety per ICH‑GCP/ISO 141155, serving as primary site contact, managing queries, supporting Trial Master File activities, and attending investigator meetings.

Premier Research seeks a Clinical Research Associate II to join its Global Clinical Monitoring and Site Management team. The role involves monitoring Phase I‑IV trials across neuroscience, oncology, rare, and cardiovascular studies, ensuring data integrity per ICH‑GCP/ISO 141155, and serving as the primary contact for investigative sites.

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 team at Merck conducts ophthalmology trials across the United States. The Senior Clinical Research Associate manages site relationships, ensures protocol compliance, and leads monitoring activities both remotely and on‑site, mentoring junior CRAs.

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.

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

Senior Clinical Research Associate at IQVIA responsible for monitoring clinical trial sites across multiple U.S. locations. Conducts site visits, ensures compliance with GCP and ICH, manages protocol training, and oversees recruitment, enrollment, and data collection.

Parexel FSP team drives clinical research excellence, transforming scientific discoveries into new treatments. As a Senior Clinical Research Associate you will manage site activities and supervise oncology studies for a single client, mentor junior CRAs, and ensure compliance with GCP/ICH standards while working from your home office in Poland.

Worldwide Clinical Trials (WCT) is a global CRO advancing patient care through clinical research. As a Contractor Senior Clinical Research Associate, you will manage non-interventional studies across cardiovascular, metabolic, CNS, oncology, and rare disease sites, overseeing start‑up, site training, data collection, and regulatory compliance.

Graduate Research Associate apprenticeship providing research experience in biomedical informatics, including bioinformatics, translational bioinformatics, imaging informatics, clinical research informatics, clinical/medical informatics, and public health informatics. Requires enrollment in an OSU degree program.

Graduate Research Associate in the Biomedical Informatics program at The Ohio State University. The role engages in mentored research across bioinformatics, translational bioinformatics, imaging informatics, clinical research informatics, and public health informatics.

Graduate Research Associate provides apprenticeship experience with financial support, complementing graduate program. Responsibilities include applying research concepts, conducting experiments, analyzing data, writing reports, presenting findings, collaborating on publications, and performing institutional research.

Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr-accessibleapplication@osu.edu .

Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr-accessibleapplication@osu.edu .

IQVIA Biotech seeks a dedicated Clinical Research Associate (CRA) to monitor and manage clinical sites across multiple U.S. locations. The role involves conducting site visits, ensuring compliance with GCP and ICH guidelines, and maintaining regulatory documentation.