Nexa Trials Clinical Coordinator Role

Join Nexa Trials as a Clinical Research Coordinator in Markham, Ontario, to transform eSource workflows within Canadian research sites. This hands-on, hybrid position is vital for operational success.
As a Clinical Research Coordinator, you will support site coordinators in adapting to NexaSource technology. Your expertise in clinical operations will enhance study workflows and ensure that data management practices comply with Good Clinical Practice (GCP). You'll engage with both local site teams and centralized analysts to streamline operations and maintain compliance.
Key Responsibilities:
• Train coordinators on NexaSource forms and visit schedules
• Assist during startup phases by confirming protocol details
• Track visit completion and manage source documentation
• Confirm field mappings for eSource-to-EDC transfer readiness
• Facilitate GCP documentation coaching sessions
Requirements:
• 3–5 years' clinical research experience on Phase I–IV trials
• ...