Clinical Research Coordinator
Support Canadian research sites adopting NexaSource and centralized QC — training coordinators, monitoring visit completion, and partnering with PI teams on live studies.
Six roles across clinical operations, data, AI, quality, and commercial growth. Select a position to read the full job description and apply.
Support Canadian research sites adopting NexaSource and centralized QC — training coordinators, monitoring visit completion, and partnering with PI teams on live studies.
Design clinical data models, EDC/eSource mappings, and integration schemas that power Nexa Bus automation and sponsor reporting pipelines.
Build LLM-assisted mapping, document extraction, and workflow automation that accelerates eSource-to-EDC transfers without compromising GCP traceability.
Execute centralized source-to-EDC quality checks, query management, and audit-ready documentation for multi-site sponsor programs in the GCC.
Execute centralized source-to-EDC quality checks, query management, and audit-ready documentation for multi-site sponsor programs across global regions.
Own enterprise pipeline for site networks and mid-size sponsors — positioning Nexa automation, NexaSource, and QC services across the United States.
Don't see a fit? We welcome general interest from exceptional clinical, data, and engineering talent.