Clinical Research Associate Jobs in Tennessee, United States

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.

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.

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.

Premier Research’s Global Clinical Monitoring and Site Management team builds the bridge between biotech, medtech, and specialty pharma companies and the patients who need new medicines. As a Clinical Research Associate I, you deliver quality monitoring reports, conduct site visits—remote or on‑site—ensuring data integrity and patient safety, and collaborate with the Clinical Lead to proactively resolve trial issues.

Thermo Fisher Scientific Clinical Research team conducts multi‑therapeutic clinical trials across the US Southeast and West regions. The Clinical Research Associate II coordinates remote and on‑site monitoring, ensures protocol compliance, manages documentation, and supports site relationships.

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.

Thermo Fisher Scientific Clinical Research team advances oncology and genetic medicine trials worldwide. The Clinical Research Associate conducts remote and on‑site monitoring visits, ensures protocol and regulatory compliance, manages documentation, and builds collaborative relationships with investigational sites.

Senior Clinical Research Associate (Level II) at Thermo Fisher Scientific. Lead remote and on‑site monitoring of clinical trials, ensuring protocol compliance, ICH‑GCP adherence, and data integrity.

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.

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.

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.

Peredo Lab in the Department of Special Education at Vanderbilt University leads innovative early intervention research for Latino families. The Senior Research Associate directs an NIH Phase 1 clinical trial, overseeing protocol implementation, bilingual caregiver coaching, REDCap data management, and a multidisciplinary research team.

The Clinical Research Coordinator at Sarah Cannon Research Institute (SCRI) plays a pivotal role in managing the clinical operations of the institute’s research program. Responsibilities include enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up, reviewing study design and inclusion/exclusion criteria with physicians and patients, and ensuring informed consent procedures are properly documented.

Research Nurse at Tennessee Oncology supports clinical trials by screening, enrolling, and monitoring study subjects. Responsibilities include obtaining informed consent, documenting adverse events, dispensing oral investigational products, and ensuring protocol compliance.

Business Development (BD) team at Thermo Fisher Scientific drives growth for Trialmed Early Phase clinical research services. The Associate Account Director manages the full sales cycle—from cold‑calling and client visits to proposal development, negotiation, and contract closure—ensuring client satisfaction and meeting revenue targets.

IQVIA, a global leader in clinical research and healthcare intelligence, seeks an Associate Program Manager, Affordability to oversee daily operations of a dedicated copay support call center team. The role ensures timely completion of tasks, compliance with SOPs and SLAs, and alignment of KPIs with daily activities.