This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Clinical Research Associate based in Canada.

This is an opportunity for an experienced clinical research professional to contribute to the successful delivery of Phase II and III clinical studies across Canada.
You will take ownership of on-site monitoring activities while ensuring high standards of data quality, patient safety, and regulatory compliance.
The role offers exposure to a broad range of clinical research activities and the opportunity to work closely with sites, vendors, and cross-functional project teams.
You will serve as a key point of contact for clinical sites, supporting effective communication and study execution throughout the trial lifecycle.
Your expertise will also contribute to feasibility activities, regulatory submissions, audits, and inspections.
Working in a dynamic and collaborative environment, you will have the autonomy to manage priorities while partnering with experienced clinical research professionals.
This role is particularly suited to someone looking to broaden their therapeutic experience and further develop their expertise in clinical research.

What the job really is