Clinical Research Coordinator

What this role involves

The Clinical Research Coordinator will manage and execute Phase II-IV clinical studies at a research site in Lake Worth, FL. Responsibilities include coordinating all aspects of trials, conducting subject visits, ensuring compliance with GCP/ICH and FDA regulations, and collaborating with investigators and sponsors. The role is onsite and full-time.

Skills this posting asks for

• clinical research coordination
• patient recruitment
• informed consent
• data entry
• electronic data capture
• phlebotomy
• ecg
• sample processing
• regulatory compliance
• good clinical practice
• ich guidelines
• fda regulations
• adverse event reporting
• protocol management
• site management

Requirements

• Level: mid
• Remote policy: onsite

From the employer’s posting

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Found…