Clinical Research Coordinator I - Nurse

Responsibilities

• Communicate study requirements to all individuals involved in the study
• Develop and implement recruitment strategies in accordance with IRB requirements
• Pre-screen and screen subjects for eligibility using protocol specific criteria
• Enter participant information and study visit procedures into the Clinical Trial Management System
• Maintain adequate inventory of study supplies and manage investigational drug/device accountability
• Complete study documentation including consent forms, source documentation, and case report forms
• Maintain ongoing communication with sponsors, research participants, site managers, and PIs
• Manage day-to-day study activities including problem solving and protocol management
• Collect and report patient recruitment and enrollment metrics
• Protect the rights and welfare of human research participants in accordance with Federal regulations
• Cooperate with compliance and monitoring efforts regarding PHI

Requirements

• RN license required

Preferred Qualifications

• 1-3 years of Clinical Research Coordinating experience

About the Company

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes through a global network of clinical research sites and cutting-edge AI.