Clinical Research Coordinator I - Nurse

The role

The CRC-RN supports, facilitates and coordinates the daily clinical trial activities. This person plays a critical role in the conduct of the study.

What you will do

• Communicate study requirements to all individuals involved in the study.
• Develop and implement recruitment strategies in accordance with GI Alliance RESEARCH and IRB requirements and approvals.
• Pre-screen and Screen subjects for eligibility using protocol specific inclusion and exclusion criteria.
• Entry of participant information and study visit procedures into the Clinical Trial Management System to ensure billing to appropriate funding sources.
• Maintains adequate inventory of study supplies.
• Follows the sponsor protocol and/or GI Alliance RESEARCH Policy on Investigational Drug/Device Accountability when handling investigational drugs/devices.
• Complete study documentation and maintenance of study files in accordance with sponsor requirements and GI Alliance RESEARCH policies and procedures.
• Maintains effective and ongoing communication with sponsor, research participants, site manager, Regional Director, and PI during the course of the study.
• Manage the day to day activities of the study including problem solving, communication and protocol management.
• Collects and reports ongoing patient recruitment/ enrollment metrics to site manager and PI.

Required qualifications

• RN license required

Nice to have

• 1-3 years of Clinical Research Coordinating experience preferred

About the company

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies.