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GCP Research: Clinical Research Nurse

GCP Research

This is a Full-time position in Montreal, QC posted April 20, 2021.

Coordinates study visits as per study protocol Executes of all aspects of study visit (e.G.

adverse events, questionnaires, sample collection, processing and shipment of samples according to clinical protocol) Responds to queries and requests for information Coordination of all aspects of data collection and source documentation, as per ICH/GCP guidelines; Maintains regulatory documents for each study Clinical evaluation of the participants according to the protocol requirements Responsible for Research Ethics Board submissions and ensures ethical approvals are continued throughout the study Timely completion of all research charts (CRF’s) Conducts other related tasks as assigned by supervisor.

* Having worked on oncology studies or having experience with chemotherapy administration is a plus.

* Must have a minimum of 2-3 years experience.

* Please submit your CV to info@montrealclinicaltrials.com