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Boston, MA, USA ● Req #260Friday, April 12, 2024We are seeking an Associate Director/Director, Data Architecture & Engineering (DA&E), to join our team. This role will be responsible for driving the development and implementation of an enterprise data strategy and architecture, including implementation of systems, tools and processes to enable critical use cases in data lineage and lifecycle management, analytics and reporting, systems integration, and process automation. The Associate Director/Director, Data Architecture & Engineering (DA&E) ...Read more about Associate Director/Director, Data Architecture & EngineeringMore
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Boston, MA, USA ● Req #258Thursday, April 11, 2024We are seeking a Senior Director/Executive Director, Customer Engagement to join our team. The individual will be an integral member of the Commercial team and will lead commercially focused customer engagement activities for XEN1101, as well as future products. The key primary responsibility is to support key US Commercial strategic market development strategies for the epilepsy launch. Individuals should be an exceptional business leader with deep epilepsy and neurology experience who will wo ...Read more about Senior Director/Executive Director, Customer EngagementMore
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We are seeking a Scientific Project Associate to join our team for a 12-month contract. The Scientific Project Associate will work flexibly across several discovery-stage small molecule programs, providing critical compound logistics and contract management support. This role will involve close coordination with stakeholders within Discovery (e.g. Chemistry, Biology, Compound Properties, Toxicology, and CMC) and outside Discovery (e.g. Shipping and Receiving, Finance, Legal). This position re ...Read more about Scientific Project AssociateMore
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Boston, MA, USA ● Req #256Wednesday, April 10, 2024We are seeking an Associate Director/Director, Quality, Regulatory & Supply Chain (QR&SC) Information Systems, to join our team. This role will be the IT business partner for the Quality, Regulatory and Supply Chain functions and will be the primary point of contact on all topics related to IT. The Associate Director/Director, Quality, Regulatory & Supply Chain (QR&SC) Information System will partner with these groups to develop and execute against a functional technology roadmap, support existi ...Read more about Associate Director/Director, Quality, Regulatory & Supply Chain SystemsMore
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Vancouver, BC, Canada ● Req #256Wednesday, April 10, 2024We are seeking an Associate Director/Director, Quality, Regulatory & Supply Chain (QR&SC) Information Systems, to join our team. This role will be the IT business partner for the Quality, Regulatory and Supply Chain functions and will be the primary point of contact on all topics related to IT. The Associate Director/Director, Quality, Regulatory & Supply Chain (QR&SC) Information System will partner with these groups to develop and execute against a functional technology roadmap, support existi ...Read more about Associate Director/Director, Quality, Regulatory & Supply Chain SystemsMore
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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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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 dynamic, experienced Senior Director/Director, Marketing (HCP) to join our growing Commercial team. As part of a team of sophisticated, passionate and collaborative marketers, this individual will play a crucial role in preparing the market for and delivering the successful launch of an innovative, high-potential new therapy in the multi-billion dollar epilepsy category. More specifically, they will lead market development and healthcare provider engagement strategy and executio ...Read more about Director/Senior Director, Marketing (HCP)More
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We are seeking a Manager, Technical Writing, CMC to join our growing team. The ideal candidate should be an independent and self-directed contributor who will be responsible for converting scientific data into clear, scientifically sound, well-structured scientific, technical, and regulatory documents intended for global health authorities and internal and external stakeholders. The Manager, Technical Writing, CMC, will author and manage the review and approval of CMC regulatory documents, incl ...Read more about Manager, Technical Writing, CMCMore
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We are seeking a Manager, Technical Writing, CMC to join our growing team. The ideal candidate should be an independent and self-directed contributor who will be responsible for converting scientific data into clear, scientifically sound, well-structured scientific, technical, and regulatory documents intended for global health authorities and internal and external stakeholders. The Manager, Technical Writing, CMC, will author and manage the review and approval of CMC regulatory documents, incl ...Read more about Manager, Technical Writing, CMCMore
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We are seeking a Director/Senior Director, Market Access, to join our team. The Director/Senior Director, Market Access will be an integral member of the US Market Access team and the broader Commercial teams. They will lead the payer strategy development and tactical execution for XEN1101 and assigned future products. The Director/Senior Director, Market Access will interact with internal stakeholders on the Commercial Team, Medical Affairs, Finance, Legal, Clinical Development, and with extern ...Read more about Director/Senior Director, Market AccessMore
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Boston, MA, USA ● Req #249Monday, April 1, 2024We are seeking an Associate Director/Director, Regulatory Affairs, CMC to join our growing team. This role will develop, propose, and implement well-informed global CMC regulatory strategies in a highly cross-functional, collaborative, project team environment. The ideal candidate will be an independent and self-directed team player with strong communication and influencing skills. This position reports to the Senior Director, Regulatory Affairs, CMC and will be in Boston, MA, USA. We will cons ...Read more about Associate Director/Director, Regulatory Affairs, CMCMore
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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