Clinical Research Coordinator-259300

Medix™ · Des moines metropolitan area, United States

We are seeking a patient-focused, detail-oriented Clinical Research Coordinator to join a clinical trial team. Working closely with research assistants and site staff, you will ensure protocol compliance, real-time documentation, and exceptional participant care.

Responsibilities

• Review, master, and adhere to assigned clinical trial protocols and study workflows.
• Conduct patient visits and deliver direct patient care, spending approximately 50% of your time working directly with trial participants.
• Capture accurate, real-time documentation for all clinical procedures and study data.
• Perform routine clinical procedures, including mandatory vital signs collection (weight, height, temperature, blood pressure).
• Perform electrocardiograms and routine blood collections.
• Complete trial-related administrative duties in collaboration with research assistants and site leadership.

Required Skills

• 2+ years of hands-on clinical research experience.
• Background in direct patient care within a healthcare or clinical setting.
• Mandatory proficiency in clinical vitals collection (weight, height, temperature, blood pressure).
• Excellent attention to detail with strong real-time data documentation skills.

Preferred Skills

• Phlebotomy certification and active blood draw capabilities.
• Experience administering or managing Spanish consent forms.