
Senior Clinical Research Associate – Field Based
Posted 6 hours ago

Posted 6 hours ago
This is a fully remote position, open to applicants in Florida.
• Serve as the main point of contact for assigned sites throughout the study delivery process.
• Foster strong relationships to enhance site performance, maintain quality, and achieve milestones.
• Oversee Phase I to Phase IV clinical trials in accordance with monitoring plans and company protocols.
• Conduct site initiation visits and provide ongoing training to site personnel.
• Execute remote and on-site monitoring to ensure compliance with regulations and ensure patient safety.
• Keep accurate documentation and promptly update all clinical systems.
• Identify potential risks, address issues, and escalate concerns when necessary.
• Collaborate with cross-functional teams to facilitate smooth study execution.
• Assist in timely resolution of data queries and ensure data accuracy.
• Serve as a subject matter expert for study activities as needed.
• At least three years of experience in clinical site monitoring.
• A Bachelor’s degree in science, healthcare, or a related field is required.
• Strong knowledge of clinical research and drug development processes.
• Familiarity with ICH/GCP and 21 CFR regulatory requirements.
• Capability to manage multiple priorities and work autonomously.
• Excellent site management, communication, and problem-solving abilities.
• Proficiency in English, both written and spoken; Spanish is highly preferred.
• Willingness to drive and travel extensively, up to 80%, using a company vehicle.
• Comprehensive health, life, and disability benefits.
• 401(k) plan with company contributions and matching.
• Generous time-off package, including vacation, personal days, holidays, and other leave options.
ICON plc
MSD
Foley
Claims Management Resources, Inc. (CMR)
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