Xenon Pharmaceuticals seeks a Clinical Trial Associate I or II in Vancouver, BC. Support clinical operations through meticulous tracking and document management in a hybrid work environment. As a Clinical Trial Associate, you will assist with critical functions of clinical trial executions, including document reviews and collaboration with vendors.

Your role is pivotal in managing the administrative side of clinical studies aimed at revolutionary treatments for conditions like epilepsy. Your organizational skills will help streamline trial progress and improve research outcomes. Key Responsibilities:

- Support preparation and maintenance of clinical study documents
- Track regulatory submissions for trial sites




- Create and manage clinical trial tracking tools
- Ensure quality of electronic trial master files
- Assist in organizing investigator meetings Requirements:
- Bachelor’s degree in health sciences or comparable
- Minimum 2+ years’ relevant experience in a biotech or CRO
- Familiarity with ICH-GCP guidelines
- Solid problem-solving abilities and teamwork skills
- Proficiency in Microsoft Word, Excel, and PowerPoint Leverage your clinical trial experience to drive success at Xenon Pharmaceuticals and make a meaningful impact.

📌 Clinical Trial Associate I or II at Xenon (Burnaby)
🏢 Xenon Pharmaceuticals
📍 Burnaby