Clinical Research Associate Jobs in Tennessee, United States

Clinical Research team at St. Jude Children's Research Hospital advances pediatric treatments through rigorous study management. The Clinical Research Associate I/II maintains protocol portfolios, conducts informed consent, abstracts and enters data, prepares regulatory submissions and complex reports, and mentors new staff.

Bioethics Program at St. Jude Children’s Research Hospital builds ethical frameworks for pediatric care and research. The Clinical Research Associate II supports data abstraction, case report forms, and informed consent for studies on sickle cell, cancer, and neuromuscular disorders.

Department of Radiology at St. Jude Children's Research Hospital advances pediatric imaging to guide diagnosis and therapy monitoring. The Clinical Research Associate supports clinical research by abstracting, collecting, and entering data, preparing reports, and ensuring protocol compliance, while RN associates also provide patient care and education.

Clinical Operations at Luminate Medical designs innovative cancer care solutions. The Senior Clinical Research Associate leads site coordination for pivotal trials, managing study documents, conducting site visits, and ensuring GCP compliance.

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

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.

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.

Senior Clinical Research Associate RN on the Department of Infectious Diseases at St. Jude Children’s Research Hospital. Builds and manages clinical trial start‑up, enrollment, and day‑to‑day operations across multi‑site studies, ensuring regulatory compliance and data quality.

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.

Fortrea is seeking Experienced CRA 2s to lead and support its Full Service Outsourcing team across major US hub locations. In this role, you will apply clinical judgement to monitor clinical trial sites, ensure participant safety and data integrity, and respond to emergencies per clinical research standards.

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.

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.

Care Access Research team advances clinical studies to bring innovative health solutions to underserved communities. The Clinical Research Coordinator II manages patient screening, enrollment, and monitoring, ensures protocol compliance, conducts phlebotomy and vital sign collection, and mentors junior coordinators.

The Clinical Research Nurse (CRN) joins the Research department of a Rheumatology care organization, reporting to the Director of Research. The role manages assigned unblinded clinical trial protocols, serving as the primary pharmacy designee for unblinded trials in Arizona, preparing investigational medications for subcutaneous injections or intravenous infusions, and traveling to sites approximately 2-3 days per week.

The Clinical Research Coordinator 1 at Vanderbilt University Medical Center's Vanderbilt Coordinating Center (VCC) within the Vanderbilt Institute for Clinical and Translational Research (VICTR) coordinates approval processes and conducts research protocols to maintain research integrity and quality. Day-to-day duties include preparing IRB proposals and regulatory documents, recording data on case report forms, shipping study specimens, assisting with study closeout, and communicating with inves

Iterative Health is a healthcare technology and services company accelerating clinical research across gastrointestinal, hepatology, obesity, and cardiology. As a Clinical Research Coordinator II in Cordova, TN, you will independently coordinate daily study activities, manage complex trials from start-up through closeout, and ensure compliance with protocols, regulatory standards, and patient safety guidelines.

Lead day‑to‑day operations of a multi‑site DOSE Trial, ensuring regulatory compliance, coordinating across sites, managing IRB submissions, overseeing REDCap data, supervising staff, and maintaining protocol adherence. Hybrid remote schedule with on‑site presence at Vanderbilt Children’s Hospital.

Profound Research invites clinicians, clinical research professionals, and recent graduates to join its Talent Network, a platform to connect with future opportunities in advancing patient care through clinical research. The network seeks dynamic, mission‑driven individuals who are detail‑oriented, entrepreneurial, and operate with urgency.

The Department of Psychology and Biobehavioral Sciences at St. Jude Children’s Research Hospital in Memphis, Tennessee, is seeking a full-time Clinical Research Scientist to advance biobehavioral health outcomes for survivors of pediatric catastrophic diseases. The role conducts literature reviews, data collection and analysis, manuscript preparation, clinical intervention research, and grant development under lead faculty supervision, while also initiating independent research and assisting wit

Vanderbilt University Medical Center’s Neurology Admin 20 team seeks a Clinical Research Coordinator I in Nashville, TN, to support clinical and translational research protocols. The role involves coordinating IRB submissions, managing study documentation, collecting data, and ensuring regulatory compliance under supervision.