Kirkland, Quebec

Overview

The CRA II monitors Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. Responsibilities include conducting site visits, training personnel, and managing site activities from start-up to close-out.

Overview

Responsible for the well-being of residents and the administration of required medical care. Collaborates with nurses, doctors, and other healthcare professionals to monitor and report changes in resident health status.

Overview

The MSL is responsible for engaging in non-promotional, peer-to-peer scientific communications with Scientific Leaders and Key Decision Makers. They provide medical information, gather disease insights, and support internal medical affairs plans and clinical trial identification.

Overview

The Senior Site Activation Coordinator will execute country-level tasks related to site activation, including performing feasibility studies and managing document review, tracking, and distribution for investigative sites. This role ensures all activities comply with applicable regulations, SOPs, and project guidelines while supporting system and database maintenance.

Overview

The role involves performing monitoring and site management tasks for various clinical protocols, therapeutic areas, and sites, including conducting site visits (selection, initiation, monitoring, and close-out) according to contractual scope and regulatory guidelines. Key duties include managing protocol training, tracking study progress, ensuring data quality and integrity, and maintaining essential study documentation like the TMF and ISF.