Health Canada CTA submissions define this Site Start-up Associate II role at Premier Research, requiring regulatory expertise and accurate document management. Support clinical study activation across Canada.

As a Site Start-up Associate II, you prepare Health Canada CTA Applications and other required local or hospital submissions. You forecast timelines, resolve country-level EC, IRB, or CA issues, and review essential documents against sponsor, investigator, local regulatory, and ICH/GCP requirements. You also support informed consent and patient documentation.

Key Responsibilities:

- Prepare and submit Health Canada CTA Applications
- Forecast submission and approval timelines
- Resolve country-level EC, IRB, or CA issues




- Review essential documents for regulatory compliance
- Adapt informed consent and patient document templates

Requirements:

- Undergraduate degree in clinical, science, or health-related field
- Three or more years of direct study start-up experience
- Working knowledge of Health Canada submissions and regulations
- Knowledge of country-specific clinical trial requirements
- Ability to work independently within agreed timelines

Apply regulatory submission expertise, document review, and clinical start-up knowledge as a Health Canada CTA specialist at Premier Research.

📌 Health Canada CTA Submission Associate (Ottawa)
🏢 14 Premier Research Group Canada
📍 Ottawa