Clinical Research Coordinator - Ocala, FL

Clinical Research Coordinator - Ocala, FL
Work Set-Up: On-site
Scheduled Weekly Hours: 24 Hours per week

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to drive healthcare forward. By combining deep scientific expertise with cutting-edge technology, we deliver high-quality data and insights that accelerate innovation and improve patient outcomes worldwide.

About the Role

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.

Key Responsibilities

• 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.

Qualifications

• Bachelor’s degree preferred, or an equivalent combination of education and relevant experience.
• 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.

Please note: This position is not eligible for sponsorship.