Clinical Research Coordinator - Ocala, FL

Benefits

Qualifications

• •Minimum of 1+ year of experience in clinical research or a related healthcare setting
• •Working knowledge of clinical trials, GCP principles, and medical terminology
• •Experience conducting study visits, including patient education and chart review
• •Exposure to related clinical procedures is required
• •Familiarity with maintaining regulatory binders, managing study supplies, and updating study portals
• •Strong attention to detail with the ability to build effective working relationships
• •Proficiency in EDC systems, accurate data entry, and query resolution
• •4 more items(s)

Responsibilities

• •Scheduled Weekly Hours: 24 Hours per week
• •We are seeking a Clinical Research Coordinator (CRC) to support clinical research studies under the supervision of a Principal Investigator
• •This role plays a critical part in the successful execution of clinical trials, combining hands-on clinical procedures, patient interaction, and study coordination to ensure compliance, data integrity, and participant safety
• •Perform clinical procedures including ECGs, vital signs, and biological sample collection
• •Coordinate daily clinical research activities in compliance with study protocols and Good Clinical Practice (GCP) guidelines
• •Prepare and maintain study materials, equipment, and documentation to support study conduct
• •Recruit, screen, consent, and orient study participants, ensuring a positive and safe patient experience throughout the trial
• •Accurately collect, document, and enter clinical data into case report forms (CRFs) and electronic data capture (EDC) systems
• •Collaborate closely with investigators, monitors, and study team members to resolve queries and maintain data quality
• •Serve as a patient advocate while maintaining a safe clinical environment in accordance with Health and Safety policies
• •7 more items(s)