Clinical Research Associate Jobs in Florida, 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.

Department of Psychiatry at the University of Miami conducts cutting‑edge clinical research on neuropsychiatric disorders. The Clinical Research Associate 3 coordinates complex study protocols, develops SOPs, oversees recruitment, manages sample logistics, and ensures regulatory compliance.

The Phase I team at Fortrea is seeking a Clinical Research Associate II to provide high standards of care for participants in clinical trials and respond to emergency situations based on clinical research standards. Day-to-day, you will handle all aspects of study site monitoring, site management, informed consent verification, CRF review and query resolution, SAE reporting, and may coordinate clinical projects as a Local Project Coordinator.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate, CNS, manages site activities from start‑up through close‑out, conducts initiation visits, ensures regulatory compliance, and supports data collection remotely while traveling regionally as needed.

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 team at Worldwide Clinical Trials drives multi‑therapeutic clinical studies, including oncology, by managing site activities and ensuring regulatory compliance. The Senior Clinical Research Associate oversees site start‑up, conducts study initiation visits, trains sites, monitors safety and data, and closes studies, collaborating remotely with sites across the Southeast and Mid‑Atlantic.

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.

The Clinical Research team is seeking a graduate-level student to assist with project and operational support while gaining hands-on experience in clinical research processes, study management, data quality initiatives, and research operations. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™.

The Clinical Research Associate typically reports to the principal investigator of a clinical research study. The position may perform evaluation duties in preparation for the project.

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.

The Clinical Research Associate will function as the main point of contact for assigned sponsored and investigator-initiated studies. The CRA II will perform investigator site management activities in adherence to all applicable regulatory guidelines and standard operating procedures (SOPs) including site GCP compliance, trouble shoot issues and facilitate resolution, and monitor safety at the site.

Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance. Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials.

Our Phase I team is currently seeking a Clinical Research Associate with 1+ years of experience. Ideal candidates would have phase I experience and reside in the Florida.

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture.

Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance. Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials.

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.

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

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.

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.

The FSP Clinical Research Associate (Level I & Level II) role supports respiratory and cardiovascular clinical trials across the Southeast region, coordinating clinical monitoring and site management for a global team that has supported top pharmaceutical and biotech sponsors. Day-to-day, you will conduct remote or on-site visits to assess protocol and regulatory compliance, manage documentation, ensure audit readiness, and develop collaborative relationships with investigational sites while adh