Clinical Research Associate Jobs in Florida, United States

The University of South Florida seeks a Clinical Research Associate to oversee regulatory components and participant management for clinical trials in Tampa, FL. This on-site role involves coordinating study visits, ensuring data quality, and maintaining compliance with federal regulations under the direction of the Principal Investigator. The position supports both sponsored and investigator-initiated studies through rigorous protocol adherence.

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

Novartis Clinical Operations team ensures high‑quality data delivery for Phase I‑IV trials. The Senior CRA monitors assigned sites, conducts initiation visits, performs continuous onsite or remote monitoring, and collaborates with project managers and internal stakeholders to resolve data queries and ensure compliance with ICH/GCP and FDA regulations.

AbbVie's Clinical Research Associate II in Orlando, Florida, advances the company's pipeline by ensuring high-quality clinical trial execution and site engagement. Day-to-day, the role serves as the primary point of contact for investigative sites, conducting monitoring visits, training site staff, assessing risks, and ensuring protocol and regulatory compliance.

Merck seeks a Clinical Research Associate to manage assigned protocols and sites within Immunology, ensuring compliance with ICH/GCP and country regulations. The role involves acting as the primary site contact, performing remote and on-site monitoring, and developing new clinical research territories across designated US locations.

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.

Clinical Research team at Merck conducts cardiovascular trials to advance therapeutic innovation. The CRA ensures protocol compliance, manages site relationships, and performs remote and on‑site monitoring while coordinating with cross‑functional groups.

Clinical Research team at Merck conducts cardiovascular studies, ensuring protocol compliance and patient safety across multiple sites. The Clinical Research Associate manages site relationships, performs remote and onsite monitoring, and collaborates with cross‑functional groups to drive study execution.

Research Support at University of South Florida collects and manages patient and laboratory data for clinical studies, overseeing screening, enrollment, and regulatory reporting. The role coordinates site visits, ensures data quality, and collaborates with social workers and health agencies to support participants.

AbbVie’s Neuroscience team seeks a Clinical Research Associate II in Tampa, Florida, to advance its pipeline by ensuring excellence in clinical research and turning science into medicine. The role involves partnering with investigators, conducting site monitoring for data integrity and compliance, and mentoring junior staff within the neuroscience therapeutic area.

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 Research Associate I – Thermo Fisher Scientific, part of the global clinical operations team that supports pharmaceutical and biotech trials. The role conducts remote and on‑site monitoring visits, ensures protocol compliance, manages documentation, and collaborates with investigative sites to maintain data integrity.

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.

Merck seeks a Clinical Research Associate to manage site performance and compliance for assigned protocols in Immunology. The role involves monitoring clinical trials, ensuring ICH/GCP adherence, and developing new site relationships across the US. This is a fully remote position requiring significant domestic and international travel.

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.

Clinical Research team at Merck drives cardiovascular, vaccine, and infectious disease studies. The Clinical Research Associate monitors site compliance, manages study documentation, and builds strong site relationships across the United States.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas, including rare CNS diseases. The Senior Clinical Research Associate manages site activities from start-up to closeout, conducts initiation visits, ensures regulatory compliance, and supports data collection remotely.

Clinical Research Associate on the Cardiovascular/Vaccine/Infectious Disease team at Merck, responsible for ensuring protocol compliance and site performance across multiple US locations. The role monitors clinical sites, manages relationships, conducts site visits, and oversees data quality and patient safety while collaborating with cross‑functional teams.

Department of Executive Dean of Research at University of Miami oversees clinical trial safety. The Clinical Research Safety Associate ensures compliance by reviewing adverse event reports, maintaining safety databases, and drafting regulatory narratives.

Clinical Monitoring team at Rho drives successful clinical trials by ensuring site compliance and data integrity. The CRA conducts site visits, monitors protocol adherence, and mentors junior staff while coordinating extensive travel across Florida.