Lead clinical site activation across Canada using regulatory expertise, CTMS knowledge, and exact document management for Parexel FSP trials. This remote role serves regional sites.

As a Regional Site Start Up II, you will deliver activation activities across clinical trials and address geographic-specific needs. You will coordinate essential documents, regulatory packages, submissions, and timelines while collaborating with sites, sponsors, and internal teams. Your work supports compliant, inspection-ready study start-up.

Key Responsibilities:

- Deliver assigned site activation timelines according to plan
- Gather essential documents and sponsor-specific materials
- Maintain site intelligence and activation updates in CTMS




- Ensure regulatory packages meet country and ICH-GCP requirements
- Troubleshoot regional challenges and escalate activation risks

Requirements:

- Bachelor's Degree minimum education requirement
- Three to four years of relevant experience
- Experience working with the United States and Canada
- Clinical drug development and study start-up experience
- Knowledge of CTMS, TMF, and regulatory guidelines

Apply clinical start-up, regulatory, CTMS, and stakeholder collaboration skills to activate Parexel FSP sites across Canada.

📌 Regional Clinical Site Start-Up Specialist (Canada)
🏢 Parexel
📍 Canada