Xenon Pharmaceuticals Inc.

HQ
Vancouver
Total Offices: 2
394 Total Employees

Jobs at Xenon Pharmaceuticals Inc.

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3 Days AgoSaved
Hybrid
Vancouver, BC, CAN
Biotech • Pharmaceutical
The Executive Director, Total Rewards will lead total compensation strategies to attract and retain talent, managing salary, benefits, and recognition programs in a strategic HR role.
5 Days AgoSaved
Hybrid
Vancouver, BC, CAN
Biotech • Pharmaceutical
The Manager/Senior Manager will lead data management for clinical trials, oversee vendors, design databases, and ensure compliance with regulations.
5 Days AgoSaved
Hybrid
Vancouver, BC, CAN
Biotech • Pharmaceutical
Manage clinical trials for multiple Phase 3 studies, ensuring collaboration with teams, vendor management, adherence to regulations, and effective timelines. Train new staff and oversee trial best practices.
7 Days AgoSaved
Hybrid
Vancouver, BC, CAN
Biotech • Pharmaceutical
Develop and execute internal communications strategies and multi-channel programs to build culture and align employees with company mission. Create content for intranet, companywide emails, town halls, and leadership meetings. Lead planning and execution of large- and small-scale corporate events and leadership offsites, manage vendors, budgets, contracts, and invoices. Partner with stakeholders globally to drive engagement, brand consistency, and process improvements. Support Corporate Affairs initiatives and occasional international travel; role is hybrid based in Vancouver with in-office event responsibilities.
8 Days AgoSaved
In-Office
Vancouver, BC, CAN
Biotech • Pharmaceutical
Provide administrative and project coordination for Discovery teams; manage ingestion, organization, and distribution of externally generated scientific data into ELN and enterprise systems; maintain records and inventories; support lab and meeting logistics; collaborate with IT and scientific teams to improve workflows and ensure compliance and safety.
Biotech • Pharmaceutical
Provide scientific leadership for clinical study design, execution, analysis, and reporting across assigned neuroscience programs. Support protocol development, safety and efficacy data review, regulatory documentation, cross-functional collaboration with CROs and partners, investigator interactions, and development of SOPs and study materials to ensure scientifically rigorous, operationally feasible clinical development.