Support clinical trial launches remotely from Canada through Health Canada submissions and accurate regulatory documentation coordination. Help activate studies across international research projects. As a Study Start-Up Coordinator, you will facilitate regulatory and administrative activities across clinical trials, therapeutic areas, and study phases. You will coordinate with clinical research sites, internal teams, and external stakeholders while maintaining compliance with Canadian regulations, ICH-GCP guidelines, and study timelines. This position contributes to accurate, efficient study activation.

Key Responsibilities:

Serve as primary contact for clinical research sites

Prepare and submit clinical trial applications to Health Canada

Review regulatory documents for compliance with Canadian requirements





Track essential documentation and monitor submission progress

Advise study teams on evolving regulatory obligations

Requirements:

Bachelor's degree in scientific, life sciences, or health discipline

Three to five years of clinical research experience

Hands-on Health Canada and Research Ethics Board submission experience

Knowledge of ICH-GCP and local clinical research regulations

Strong organization, communication, and remote collaboration skills

Apply your Health Canada submissions, site coordination, and regulatory expertise to support accurate clinical study activation across Canada.

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📌 Clinical study coordinator (Toronto)
🏢 Jobgether
📍 Toronto