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Required Skills: Proficiency with computer applications such as Microsoft applications, email, and web applications, and the ability to type proficiently (40+ wpm); Strong organizational skills and attention to detail. Essential Job Duties: In collaboration with other members of the clinical research site teamwork to ensure the entry of clinical visit data in EDC and other clinical data software/systems.

Alcanza Clinical Research LLC

Data Entry Coordinator

Job Description: The Clinical Research Office (CRO) in the Office of Research Affairs (ORA), Dean's Administration, College of Medicine-Jacksonville, is seeking a Clinical Research Analyst II to work as a CTMS Specialist, to support clinical trial operations and protocol management within the University of Florida's Clinical Trials Management System (CTMS). The Clinical Research Analyst II provides technical support and guidance to study teams regarding the use of the CTMS and institutional processes, assists with coverage analysis activities, and supports workflow management to ensure timely and accurate completion of assigned tasks.

Regulatory Coordinator Jobs in Jacksonville, FL

Data Entry Coordinator Alcanza Clinical Research LLC

Clinical Research Analyst II-Clinical Trial Mgmt Specialist University of Florida

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