Clinical Research Coordinator I, II, or III

What this role involves

The Clinical Research Coordinator role involves managing Phase I-IV clinical studies, subject visits, and regulatory compliance at a research site in Portland, OR. The position is full-time and onsite, with responsibilities including subject recruitment, data entry, and collaboration with investigators and sponsors.

Skills this posting asks for

• clinical trial coordination
• gcp
• ich guidelines
• fda regulations
• irb policies
• patient recruitment
• informed consent
• data entry
• edc query resolution
• adverse event reporting
• regulatory documentation
• phlebotomy
• ecg
• sample processing

Requirements

• 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…