Xenon Pharmaceuticals Inc.

Needham
394 Total Employees

Xenon Pharmaceuticals Inc. Benefits Overview

Compensation + Benefits

Offers 401(K)

Offers life insurance

Offers company equity

Offers performance bonuses

Offers dental insurance

Offers health insurance

Offers Flexible Spending Account (FSA)

Offers vision insurance

Offers generous parental leave

Work-Life Balance + Wellbeing

Offers company-sponsored outings

Offers an Employee Assistance Program (EAP)

Offers generous PTO

Provides paid sick days

Provides paid holidays

Provides bereavement leave

Career Growth + Development

Provides customized development tracks

Provides tuition assistance

Biotech • Pharmaceutical
Serves as the strategic HR Business Partner to Commercial Sales and Marketing leadership. Leads workforce planning, organizational design, talent strategy, sales hiring, onboarding, employee engagement, performance management, succession planning, and organizational development. Acts as HR lead for launch readiness, coordinating Talent Acquisition, Total Rewards, HR Operations, Learning and Development, Compliance, and Legal. Advises leaders through rapid growth, commercialization, organizational change, and infrastructure development while supporting an inclusive, high-performing culture.
Biotech • Pharmaceutical
Provides GCP and GLP quality assurance support for early-stage clinical programs, including quality planning, risk assessments, audits, inspection readiness, compliance consultation, training, CAPA evaluation, root cause analysis, and regulatory inspection support. Collaborates with cross-functional stakeholders to identify and escalate quality issues, maintain data integrity, and advance GLP/GCP quality strategies across pharmaceutical R&D programs.
Biotech • Pharmaceutical
Manages end-to-end clinical supply activities, including study-specific planning, forecasting, packaging, labeling, distribution, inventory monitoring, accountability, returns, and destruction. Coordinates with clinical, regulatory, quality, CMC, supply chain, and external vendors to ensure compliant and timely site supply. Oversees IXRS specifications and monitoring, vendor budgets, supply releases, documentation, KPI reporting, root-cause analysis, and continuous improvement across international clinical trials.