Senior Clinical Research Associate

PXL FSP has an exciting opportunity for a Sr. CRA with Oncology experience in the Montreal/Quebec area!

The SrCRA is responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with AZ Procedural Documents, international guidelines such as ICH‑GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.

Typical Accountabilities

• Contributes to the selection of potential investigators.
• In some countries, as required, SrCRAs are accountable for study start‑up and regulatory maintenance. Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start‑up and for the duration of the study.
• Trains, supports and advises Investigators and site staff...