Jobs at Xenon Pharmaceuticals Inc.

The Associate Director of Scientific Communications will develop and review materials for medical and congress events, ensuring alignment with scientific standards. The role involves translating complex data into clear narratives, collaborating with various stakeholders, and maintaining compliance. Success depends on a strong scientific foundation and the ability to work in a fast-paced environment.

The Associate Director/Director of Quality Assurance for GCP will oversee quality activities related to clinical development programs, manage audits, ensure regulatory compliance, and lead quality initiatives across the company.

The Director of Pricing and Contracting will develop and implement U.S. pricing strategies and payer contracting frameworks while collaborating cross-functionally to ensure successful market access and financial performance for Xenon's products.

The Senior Manager, Trial Operations will lead and manage multiple clinical trials, ensuring operational excellence and collaboration across teams in clinical project life cycles.

Manage the end-to-end supply chain strategy, ensuring compliance and efficiency from clinical development to commercialization, while leading cross-functional teams and optimizing processes.

The Director, Forecast & Research will lead forecasting, market research, and insights generation for Xenon's epilepsy portfolio, collaborating with cross-functional leaders to deliver actionable analytics.

The Senior Manager will oversee regulatory submission processes, manage external publishing vendors, support project teams, maintain regulatory calendars, and enhance operational functions within the Regulatory Affairs department.

The Senior Manager/Associate Director, Access Marketing will execute the azetukalner access strategy, develop payer value proposition, and manage patient access materials, collaborating with internal and external stakeholders.

The Statistical Programmer will lead programming support for clinical data analysis, ensuring compliance, managing CROs, and developing automation tools. Requires SAS expertise.

Lead global supply chain logistics for small-molecule clinical and future commercial programs. Oversee import/export trade compliance, customs brokers, freight forwarders, 3PLs, warehousing, distribution, KPI reporting, budgeting, continuous improvement, and team development to ensure timely delivery to patients and regulatory compliance.