Burlington, Prince Edward Island

Overview

Accountable for site selection and study start-up activities for Phase I-IV trials, ensuring timelines and deliverables are met. Manages regulatory submissions, site documentation, and financial contracts to achieve site greenlight.

Overview

The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.

Overview

The Clinical Research Associate will monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. They will also collaborate with cross-functional teams to manage data collection, site performance, and stakeholder relationships.

Overview

The Informed Consent Writer is responsible for creating health-literate informed consent documents for clinical trials across various therapeutic areas. This includes collaborating with protocol authors and managing the design and planning of documentation to ensure timely delivery and regulatory compliance.