Clinical Research Associate Jobs in North Carolina, United States

IQVIA Early Clinical Development team drives Phase 1 trials across diverse therapeutics. The Senior CRA monitors sites, ensures GCP compliance, tracks enrollment, manages TMF/ISF, and collaborates with cross‑functional teams in Durham, NC, onsite.

IQVIA’s Clinical Research team drives site monitoring and data integrity for clinical trials. The Associate conducts GCP‑compliant site visits, manages recruitment plans, and ensures accurate CRF submission.

Worldwide Clinical Trials is a global, midsize CRO on a mission to improve lives by taking pioneering, creative approaches to clinical research. As a Clinical Research Associate, you will support clinical trial operations and contribute to the company's goal of changing how the world experiences CROs.

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.

IQVIA’s Clinical Research team drives site monitoring to ensure compliance with GCP and ICH. The role conducts site visits, manages recruitment plans, and maintains Trial Master Files. Based in Overland Park, KS with additional sites in Durham, NC; Parsippany, NJ; and Carlsbad, CA, the position is on-site with a hybrid travel component.

Clinical Operations at Worldwide Clinical Trials drives scientific breakthroughs by managing multi‑therapeutic clinical studies. The Clinical Research Associate II, Psychiatry, oversees site activities, conducts initiation visits, ensures regulatory compliance, and trains sites on data collection, all while supporting psychiatric monitoring.

Fortrea's FSP team is seeking a Clinical Research Associate 2 for the West Region to deliver high-standard clinical trial monitoring and participant care across the western United States. Day-to-day work includes full-cycle site monitoring (routine and close-out visits, pre-study/initiation visits, study file maintenance), CRF review and query resolution, SAE reporting, registry management, and acting as a local project coordinator or client contact.

Perform site monitoring visits, manage study progress, ensure compliance with GCP/ICH, maintain TMF/ISF, generate reports, support recruitment, handle financials, and collaborate with study teams.

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

IQVIA is seeking a Clinical Research Associate, Sponsor Dedicated, Oncology to ensure study sites operate smoothly and advance groundbreaking research. Day-to-day duties include conducting site visits, tracking recruitment and study progress, maintaining regulatory documentation, and mentoring clinical staff.

Clinical Operations at Worldwide Clinical Trials drives innovative CRO solutions across therapeutic areas. The Senior Clinical Research Associate manages site activities for CNS and Oncology studies, conducts initiation visits, ensures regulatory compliance, and supports contract and budget negotiations, primarily remotely while residing in the Midwest.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate manages site activities, conducts study initiation visits, and ensures regulatory compliance while supporting data collection and safety reporting.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas, including Oncology. The Clinical Research Associate II manages site activities, conducts study initiation visits, and ensures regulatory compliance while supporting data collection and safety reporting.

FSP team seeks a Senior Clinical Research Associate II, Oncology to oversee clinical trial monitoring and site management. The role conducts site visits, ensures protocol compliance, reviews CRFs, and handles adverse event reporting while coordinating with vendors and training staff.

Worldwide Clinical Trials’ Clinical Operations team drives oncology studies across the East Coast. As a Senior Clinical Research Associate, you’ll qualify sites, conduct initiation visits, manage day‑to‑day site activities, and ensure timely data and safety reporting.

Worldwide Clinical Trials is a global midsize CRO advancing clinical research across therapeutic areas including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. As a Senior Clinical Research Associate in Clinical Operations, you will manage site research activities across all study stages—from site identification and start-up to maintenance and close-out—while conducting study initiation visits and ensuring regulatory compliance.

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.

Worldwide Clinical Trials Clinical Operations team drives innovative CRO solutions across therapeutic areas. As a Senior Clinical Research Associate you will manage site activities for CNS and Rare Disease studies, conduct start‑up, monitoring and close‑out tasks, and ensure regulatory compliance while primarily working remotely.

We’re looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role, you’ll partner with investigative sites and cross-functional teams to ensure studies are executed with excellence, compliance, and patient focus.