Description

You will coordinate and implement clinical research protocols in compliance with FDA CFR, GCP, and company SOPs. You will manage patient recruitment, screening, data collection, and study documentation while serving as a liaison between patients, physicians, and vendors.

Requirements

• Experience as Clinical Research Coordinator II or III
• Knowledge of FDA CFR, GCP, and clinical trial management
• Ability to perform phlebotomy and basic lab tests
• Strong organizational and data management skills
• Excellent communication and patient service skills

Responsibilities

• Manage conduct of clinical research activities under PI direction
• Recruit and screen potential study participants
• Record and maintain clinical research data and study documentation
• Serve as liaison to physicians, employees, and third-party vendors
• Ensure compliance with FDA CFR, GCP, and company SOPs