Clinical Research Associate Jobs in Kentucky, 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.

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.

The Clinical Research Associate will oversee site monitoring and management to ensure compliance with study protocols, regulations, and sponsor requirements. Responsibilities include conducting site visits, tracking recruitment, evaluating site practices, and managing study documentation.

The Clinical Research Associate (CRA) at AstraZeneca’s Cell Therapy team ensures local study sites meet ICH‑GCP and AstraZeneca SOPs. Day‑to‑day duties include monitoring visits, source data review, and maintaining eTMF and CTMS records.

Clinical Research Team at Parezon conducts oncology clinical trials to develop new therapies. The Clinical Research Associate I manages site relationships, performs monitoring visits, ensures protocol compliance, and documents study activities.

Clinical Research Associate II at St. Jude Children’s Research Hospital supports the BMT program by collecting and abstracting clinical data, maintaining case report forms, and ensuring protocol compliance. The role coordinates informed consent, prepares adverse event reports, and collaborates with site and study teams to meet research objectives.

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.

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.

We are seeking a Senior Clinical Research Associate Contractor to support clinical trials in Switzerland. The role involves site visits, report writing, regulatory tracking, and ensuring compliance with GCP guidelines.

Integrated Resources, Inc. is a leading staffing firm in the tri‑states region, specializing in IT, clinical research, rehabilitation therapy, and nursing. We are seeking a Research Associate to support the development and evaluation of new technologies using animal, inanimate, and cadaveric models.

We are seeking an experienced Oncology Clinical Research Associate (CRA) to lead and support our full-service outsourcing team. The role focuses on site monitoring, data integrity, SAE reporting, and regulatory compliance for CAR‑T trials.

VICC – Clinical Trials at Vanderbilt University Medical Center builds and maintains high‑quality clinical research data. The Associate Clinical Research Data Specialist monitors data functions, enters and reviews eligibility data, identifies adverse events, and coordinates audit deadlines for multiple studies.

Division of Translational and Clinical Pharmacology at Cincinnati Children’s Hospital Medical Center (CCHMC) seeks a tenure‑track faculty member to lead independent research in pediatric precision medicine, focusing on pharmacogenomics, multi‑omics, NAMs, pharmacometrics, and AI‑driven drug therapy optimization. The role involves developing extramural funding, collaborating across CCHMC and the University of Cincinnati, mentoring students and postdocs, and contributing to curriculum and national committees.

Jordan Lab Clinical Research Team at Vanderbilt University Medical Center conducts NIH‑funded studies on pediatric stroke, sickle cell disease, and type 1 diabetes. The Clinical Trials Associate supports participant recruitment, REDCap data entry, protocol compliance, and coordination of MRI visits, working closely with Dr. Lori Jordan and the multidisciplinary team.

Clinical Trials Associate 2 at Vanderbilt University Medical Center’s Nephrology & Hypertension Division supports clinical research by recruiting subjects, coordinating study visits, managing regulatory documents, and abstracting patient data into electronic systems. The role ensures protocol adherence, monitors enrollment, and trains new staff while driving process improvements.

Biostatistics & Epidemiology team at Cincinnati Children’s Hospital seeks a Research Associate to support data analysis and study design for pediatric clinical trials. The role involves collaborating with investigators, managing datasets, and preparing reports for regulatory submissions.

Clinical Trials Associate 2 at Vanderbilt University Medical Center works in the Pediatric Psychology team to support clinical research studies. The role coordinates protocol and consent processes, prepares IRB and regulatory documents, recruits and monitors study subjects, and abstracts patient data into electronic case report forms.

Pediatric Cardiology at Vanderbilt University Medical Center builds clinical research infrastructure to advance heart health. The Associate Clinical Data Specialist manages data capture, eligibility review, and audit readiness for Dr. Jonathan Soslow’s R01, DOD, and industry studies, ensuring data integrity and protocol compliance.