Clinical Research Associate Jobs in Tennessee, 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.

As a Clinical Research Associate II - Cardio within Worldwide Clinical Trials, you will manage research activities at sites participating in Worldwide's clinical research projects. You will work through all stages of the clinical study, including identifying potential sites, performing study start-up activities such as collecting regulatory documents and supporting contract and budget negotiations, training sites to collect data properly and report safety-related events, managing site activities

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.

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.

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.

Senior Clinical Research Associate role overseeing site monitoring, ensuring GCP compliance, guiding junior CRAs, and managing study progress across oncology trials.

Our FSP team is currently seeking Oncology CRA 2s in Southeast Region! 8-10 days on site per month being a mix of onsite and remote.

As a Clinical Research Associate II in the Department of Psychology and Biobehavioral Sciences, you will support innovative research focused on understanding brain health, cognitive function, and neurological outcomes in pediatric and adult populations. Under the direction of faculty investigators, you will coordinate and conduct research activities related to neuropsychological assessment, neuroimaging, neuromodulation, and behavioral intervention studies.

Our FSP team is currently seeking a CRA 2 with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

As a Clinical Research Associate II in the Department of Psychology and Biobehavioral Sciences, you will support innovative research focused on understanding brain health, cognitive function, and neurological outcomes in pediatric and adult populations. Under the direction of faculty investigators, you will coordinate and conduct research activities related to neuropsychological assessment, neuroimaging, neuromodulation, and behavioral intervention studies.

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.

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

The Sr. CRA II - General Medicine - East Coast or Mid-West role supports the Full Service Outsourcing team at Covance, reporting within the Fortrea Inc. organization. You will lead and support clinical trial operations by performing all aspects of study site monitoring, including routine monitoring and close-out of clinical sites, maintenance of study files, and conduct of pre-study and initiation visits.

Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, is one of the largest community-based cancer programs advancing oncology treatments and improving outcomes for cancer patients worldwide. As a Clinical Research Coordinator, you will oversee the overall clinical operations of the facility’s research program, including enrollment, regulatory, quality, and site operations.

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.

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.

Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, is one of the largest community-based cancer programs advancing oncology treatments and improving outcomes for cancer patients globally. As a Clinical Research Coordinator based in Nashville, TN, you will oversee the overall clinical operations of the facility’s research program, including enrollment, regulatory, quality, and site operations.

Care Access is a global health services and clinical research organization dedicated to making healthcare and research accessible to communities facing barriers to care. As a Clinical Research Coordinator I in Memphis, Tennessee, you will screen, enroll, and monitor clinical trial participants while ensuring protocol and regulatory compliance.

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 Radiology Department at St. Jude Children's Research Hospital seeks a Manager of Clinical Research Operations to provide overall coordination and management of clinical research workflow. The role ensures adherence to internal and external regulatory agency policies, procedures, practices, and law by all clinical research personnel.