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Boston, MA, USA ● Req #248Wednesday, March 27, 2024We are seeking a Senior Manager/Associate Director, Quality Assurance, Systems to join our team. We are building the Quality function to support Xenon’s late-stage clinical development programs and prepare for commercialization, as well as expand quality initiatives across the company. This position will be a key contributor to managing and improving Xenon’s Quality Management System. This position reports to the Director, Quality Assurance, Systems and will be in Boston, MA, USA. The level of t ...Read more about Senior Manager/Associate Director, Quality Assurance, SystemsMore
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We are seeking a Senior Director, Clinical Supplies to join our Supply Chain team. The candidate will be responsible for the Supply Chain for Clinical Supplies for a number of small molecule drug development programs in support of Xenon’s clinical trials. The Senior Director, Supply Chain, Clinical Supplies will also be responsible for managing and the end-to-end Supply Chain planning, forecasting, packaging, labeling, distribution and returns of Xenon’s products. The ideal candidate will coll ...Read more about Senior Director, Clinical SuppliesMore
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Vancouver, BC, Canada ● Req #243Monday, March 18, 2024We are seeking a Director/Senior Director, Development Program Management to lead and coordinate cross-functional planning of Xenon’s clinical-stage small-molecule drug development programs in both late and early phases with regulatory submissions experience (eg NDAs, MAAs) and life cycle management projects. This role involves close coordination with stakeholders within development (e.g., Clinical Development, Clinical Operations, CMC, Non-Clinical, Regulatory Affairs, QA) and outside of develo ...Read more about Director/Senior Director, Development Program ManagementMore
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Boston, MA, USA ● Req #243Monday, March 18, 2024We are seeking a Director/Senior Director, Development Program Management to lead and coordinate cross-functional planning of Xenon’s clinical-stage small-molecule drug development programs in both late and early phases with regulatory submissions experience (eg NDAs, MAAs) and life cycle management projects. This role involves close coordination with stakeholders within development (e.g., Clinical Development, Clinical Operations, CMC, Non-Clinical, Regulatory Affairs, QA) and outside of develo ...Read more about Director/Senior Director, Development Program ManagementMore
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We are seeking a Senior Microsoft Systems Engineer to join our team. This role will serve as the technical lead and strategist for the IT End User Computing Team. The team utilizes Microsoft Intune to manage devices and offers a variety of productivity tools centered on the Microsoft 365 platform. The Senior Microsoft Systems Engineer will serve as the technical system owner for these platforms as well as others related to productivity, messaging, collaboration, and workplace services. The succe ...Read more about Senior Microsoft Systems EngineerMore
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We are seeking a Senior Microsoft Systems Engineer to join our team. This role will serve as the technical lead and strategist for the IT End User Computing Team. The team utilizes Microsoft Intune to manage devices and offers a variety of productivity tools centered on the Microsoft 365 platform. The Senior Microsoft Systems Engineer will serve as the technical system owner for these platforms as well as others related to productivity, messaging, collaboration, and workplace services. The succe ...Read more about Senior Microsoft Systems EngineerMore
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We are seeking a Senior/Executive Director, Human Resources to join our team. The Senior/Executive Director, Human Resources will be a key member of highly collaborative HR and corporate teams, will build and lead the Learning and Development function in support of Xenon’s culture and focus on talent development, and act as a Business Partner, providing counsel, coaching and support to assigned departments, employees and managers in the U.S. and Canada. The Senior/Executive Director, Human Reso ...Read more about Senior/Executive Director, Human ResourcesMore
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We are seeking a Senior/Executive Director, Human Resources to join our team. The Senior/Executive Director, Human Resources will be a key member of highly collaborative HR and corporate teams, will build and lead the Learning and Development function in support of Xenon’s culture and focus on talent development, and act as a Business Partner, providing counsel, coaching and support to assigned departments, employees and managers in the U.S. and Canada. The Senior/Executive Director, Human Reso ...Read more about Senior/Executive Director, Human ResourcesMore
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Boston, MA, USA ● Req #239Friday, March 8, 2024We are seeking a Senior Manager/Associate Director, Quality Assurance, Systems, Training and Document Control to join our team. We are building the Quality systems function to support Xenon’s late stage clinical development programs and prepare for commercialization, as well as expand quality initiatives across the company. This position will be a key contributor to leading and managing Xenon’s Document Management and Training Management systems. This position reports to the Director, Quality As ...Read more about Senior Manager/Associate Director, Quality Assurance, Systems, Training and Document ControlMore
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Boston, MA, USA ● Req #198Friday, March 8, 2024We are seeking a Director/Senior Director, Human Resources, Systems and Data to join our team. The Director/Senior Director will be a key member of highly collaborative HR and corporate teams with responsibility for Human Resource management systems, data and reporting and for acting as a Business Partner, providing counsel, coaching and support to assigned departments, employees and managers in the U.S. and Canada. This role will represent HR as a Business System Owner, collaborating with IT a ...Read more about Director/Senior Director, Human Resources, Systems and DataMore
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We are seeking a Senior Manager, Trial Operations to join our team. This person will work flexibly across a number of clinical stage trials and projects, acting as a study lead and manager for select clinical trials, and be hands-on in data compilation, review and analysis, clinical trial set-up and management, and operational support activities. This is an excellent opportunity for someone with strong organizational skills and the ability to work independently on a variety of tasks and projects ...Read more about Senior Manager, Trial OperationsMore
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We are seeking a Clinical Trial Associate 1 to join our team. The Clinical Trial Associate 1 will be an individual responsible for supporting Clinical Operations team members with project-specific support related to the conduct of clinical trials activities. The Clinical Trial Associate 1 will assist the clinical research teams in ensuring the most effective and efficient conduct of clinical research studies by providing administrative and project tracking support. This position reports to the ...Read more about Clinical Trial Associate 1More
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Boston, MA, USA ● Req #236Friday, March 8, 2024We are seeking a Director/Senior Director, Pharmacovigilance and Drug Safety (Safety Scientist) to join our team. The incumbent is responsible for safety surveillance and aggregate safety reports and works with safety physicians for signal/risk management for assigned Xenon’s products to support product safety and compliance with global drug safety regulations and departmental procedures and provide vendor oversight to CROs. The individual authors safety documents, reviews safety sections of oth ...Read more about Director/Senior Director, Pharmacovigilance and Drug Safety (Safety Scientist)More
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We are seeking a Senior Director, Medical Affairs to join our team. The Senior Director, Medical Affairs is responsible for leadership and oversight for the Medical Education, Congress Strategy, Advisory Boards, Patient Advocacy and Operations functions. The Senior Director, Medical Affairs will play a central role and shaping and growing this critical Medical Affairs function, and will have the skills to be able to contribute to development of strategic Medical Affairs objectives. The Senior Di ...Read more about Senior Director, Medical AffairsMore
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We are seeking an Associate Director or Director, Trial Operations, to join our team. The Associate Director or Director, Trial Operations will be a key member of a highly collaborative Clinical Development team responsible for developing strategies and plans for our portfolio of clinical stage assets, with particular focus on global phase 3 and phase 1 programs. The Associate Director or Director is responsible for ensuring studies within a program are initiated, recruited, managed, and closed ...Read more about Associate Director/Director, Trial OperationsMore
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We are seeking a Manager or Senior Manager, Medical Writing to join our team. The Manager/Senior Manager, Medical Writing works flexibly across a number of preclinical and clinical stage projects, providing medical writing expertise, including data review. The role is hands on, requires frequent collaboration and excellent working relationships with various internal groups. This position reports to the Senior Director, Medical Writing, and will be in Boston, MA, USA. The level of the position wi ...Read more about Manager/Senior Manager, Medical WritingMore
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We are seeking a Senior Manager, Quality Assurance, GMP to join our team. The Senior Manager, Quality Assurance, GMP will work collaboratively with multidisciplinary teams and ensure adherence to GMP regulations and regulatory requirements in support of Xenon’s late-stage clinical development programs and NDA preparation. This position reports to the Associate Director, Quality Assurance, GMP and will be in Vancouver, BC, Canada. We will consider the following jurisdictions for exceptional candi ...Read more about Senior Manager, Quality Assurance, GMPMore
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We are seeking a Director or Senior Director, Trial Operations to join our team. The Director/Senior Director, Trial Operations will be a key member of a highly collaborative Clinical Development team responsible for developing strategies and plans for our portfolio of clinical stage assets, with particular focus on global phase 3 programs for XEN1101 and Phase I trials. The Director/Senior Director is responsible for ensuring studies within a program are initiated, recruited, managed, and clos ...Read more about Director/Senior Director, Trial OperationsMore
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We are seeking a Scientist 1 or 2, Clinical Pharmacology to join our team. This is a regular, full-time position. The scientist will work flexibly across a variety of projects and have expertise or proficiency in Pharmacokinetics (PK)/pharmacodynamics (PD) including PK study design, data analysis, data review and bioanalysis in support of the Company’s pipeline, IND/CTA and NDA submissions. Proficiency or familiarity with PK/PD modeling and physiologically based PK (PBPK) modeling is highly desi ...Read more about Scientist 1 or 2, Clinical PharmacologyMore
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We are seeking a Manager, End User Services, to join our team. This role will be responsible for ensuring an exceptional work experience across the company by limiting disruptions and enhancing productivity. This individual will lead a small team of Vancouver-based employees and a future Managed Services Provider (MSP). The team conducts support operations by utilizing a ticketing system in accordance with ITIL processes. The Manager, End User services will be responsible for endpoint management ...Read more about Manager, End User ServicesMore
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Boston, MA, USA ● Req #225Friday, March 8, 2024We are seeking a Senior Medical Director, Pharmacovigilance and Drug Safety to join our team. The incumbent will play a key leadership role in Drug Safety Pharmacovigilance, building Medical Safety and Risk Management team, responsible for safety and benefit-risk assessment of assigned Xenon products throughout the product lifecycle (from First-In-Human to post-marketing), providing strategic leadership in safety surveillance for Xenon’s clinical development programs pre- and post-launch, and en ...Read more about Senior Medical Director, Pharmacovigilance & Drug SafetyMore
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Boston, MA, USA ● Req #224Friday, March 8, 2024We are seeking an Associate Director / Director, R&D Financial Planning & Analysis to join our growing Financial Planning & Analysis team. The Associate Director / Director, Financial Planning & Analysis will lead the R&D finance function and serve as a business partner to the Discovery and Development organizations. This role will support Xenon’s growing portfolio of discovery and development programs by enabling effective financial forecasting, reporting and analysis of operating results to en ...Read more about Associate Director/Director, R&D Financial Planning & AnalysisMore
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We are seeking a Manager/Senior Manager, CMC, Drug Product to join our CMC team. The incumbent will be required to work flexibly across a number of small molecule drug development programs with an emphasis on managing outsourced Drug Product process development projects and cGMP Drug Product manufacturing campaigns. This position reports to the Senior Director, CMC, Drug Product and will be in Boston, MA, USA location. The level of the position will be commensurate with the candidate’s educatio ...Read more about Manager/Senior Manager, CMC, Drug ProductMore
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We are seeking a Senior Manager, Regulatory Affairs to join our team. This role will develop, propose and implement well-informed global regulatory strategies in a highly cross-functional, collaborative, project team environment. The Senior Manager will be the regulatory lead for clinical studies (as assigned) with the objective to obtain regulatory approvals for the initiation of clinical studies, as well as any amendments and maintenance activities for the continued conduct of clinical studies ...Read more about Senior Manager, Regulatory AffairsMore
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We are seeking a Senior Manager, Regulatory Affairs to join our team. This role will develop, propose and implement well-informed global regulatory strategies in a highly cross-functional, collaborative, project team environment. The Senior Manager will be the regulatory lead for clinical studies (as assigned) with the objective to obtain regulatory approvals for the initiation of clinical studies, as well as any amendments and maintenance activities for the continued conduct of clinical studies ...Read more about Senior Manager, Regulatory AffairsMore