Clinical Research Associate Jobs in Florida, United States

Clinical Research Associate II on the Oncology team at Thermo Fisher Scientific, responsible for risk‑based monitoring of investigator sites across the Southeast US. The role conducts remote and on‑site visits, ensures protocol and ICH‑GCP compliance, manages audit readiness, and collaborates with sponsors and site staff to resolve findings. Based in a fully remote Florida setup, the position offers flexible travel and a focus on oncology clinical trials.

Clinical Research Associate II at Thermo Fisher Scientific supports global neurology trials, coordinating remote and on‑site monitoring to ensure protocol compliance and data integrity. The role involves risk‑based site visits, root‑cause analysis, and audit readiness, while collaborating with sponsors and investigators across the U.S. Remote work based in Florida with occasional travel to sites.

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.

Clinical Research team at Merck conducts oncology trials across the United States. The Clinical Research Associate ensures protocol compliance, manages site relationships, and performs remote and on‑site monitoring while coordinating with cross‑functional partners.

Clinical Research Associate II on AbbVie’s Clinical Operations team advances the pipeline by ensuring high‑quality site execution of trials in Central Florida. The role serves as the primary point of contact for investigative sites, conducts monitoring, training, risk assessment and data integrity activities, and mentors junior CRAs.

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 immunology trials, ensuring protocol compliance and patient safety. The CRA manages site relationships, performs remote and onsite monitoring, and oversees regulatory documentation across multiple US locations.

Clinical Research Operations at Merck conducts cardiovascular, vaccine, and infectious disease trials. The Clinical Research Associate monitors site performance, ensures compliance with ICH/GCP, manages documentation, and supports site selection and expansion.

Fortrea's Clinical Pharmacology Team seeks a Clinical Research Associate II with Phase I experience in Florida to monitor clinical trials, manage site operations, ensure protocol compliance, and report adverse events. Responsibilities include site monitoring, data integrity, SAE reporting, CRF review, and training.

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.

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.

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 Monitoring Department at Ergomed, a global CRO focused on oncology and rare disease, ensures investigational sites meet rigorous standards for study conduct. The Senior Clinical Research Associate leads on‑site and remote monitoring visits across Phase 2/3 trials, trains site staff, and mentors junior monitors while supporting 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.

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.

Neurovascular division at Stryker builds innovative medical devices to improve patient outcomes. The Senior Clinical Research Associate supports end‑to‑end clinical trials, performing site monitoring, data integrity checks, and regulatory documentation while partnering with cross‑functional teams.

Senior Clinical Research Associate at Ergomed Group, a CRO specializing in oncology and rare disease. The role monitors phase 2/3 trials on-site or remotely, ensuring investigators meet regulatory and operational standards, trains site staff, and supports regulatory submissions.

CDS Dermatology team at TFS HealthScience partners with biotech and pharma to drive clinical development. The Senior Clinical Research Associate leads on-site and remote monitoring, ensures GCP compliance, reviews CRFs, manages investigational product accountability, and supports sites through issue resolution.

Research Associate 1 at the University of Miami’s Neurology department supports laboratory and clinical research projects. The role involves designing and executing experiments, collecting and analyzing data, and maintaining lab equipment.