Now Hiring: Clinical Research Coordinator for Our Client - Full-Time

Location: Orlando, Fl

Schedule: Monday - Friday, 8 AM - 5 PM (overtime as needed)

Position Overview: Our client seeks a dedicated Clinical Research Coordinator to join their dynamic team. This role is pivotal in facilitating clinical trials, from recruitment and data management to ensuring compliance with all study protocols and regulations. This position requires effective communication skills to engage with subjects and team members throughout the study process.

Key Responsibilities:

• Conduct and monitor study subject visits, ensuring strict adherence to protocols.
• Manage subjects' recruitment, screening, and enrollment, including securing informed consent.
• Administer study drugs, manage patient charts, and handle regulatory documentation.
• Record and report adverse events and maintain accurate study records.
• Prepare study-related documentation, participate in audits, and occasionally travel for business needs.

Requirements:

• Familiarity with Good Clinical Practice (GCP) and regulatory compliance.
• Experience in a clinical research coordination role is preferred.
• Proficient in detailed documentation and data entry.
• Required training includes IATA, CPR, and potentially BLS/Phlebotomy, depending on the manager's direction.

Benefits:

• Competitive compensation package with overtime eligibility.
• Opportunities for professional development and continuous training.

If you are detail-oriented and passionate about clinical research, apply today to contribute to groundbreaking studies with our esteemed client!