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Medix is sourcing an experienced RN Clinical Research Coordinator for an in-clinic, full-time role in Ontario to manage Phase III trials. The incumbent will screen participants, collect data, perform ECGs and phlebotomy, and coordinate with investigators.
Requirements include an active RN/RPN license in Ontario, BScN or equivalent, and cardiology/ICU/ER experience. Travel to the US for investigator meetings is expected, with comprehensive dental and health benefits.
This Full time on site position offers great opportunities for career growth. Our client seeks an EXPERIENCED FULL-TIME, IN-CLINIC RN Clinical Research Coordinator with research-based nursing experience in-person Phase III Clinical Trials.
Ability to think, problem solve, prioritize, demonstrate proficiency in computer communications, self-directed, independent work. Demonstrated excellence in communication, organization, & collaboration.
The nurse will coordinate clinical trials.