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Boston, MA, USA ● Req #306Wednesday, January 15, 2025We are seeking a Senior Manager, Regulatory Affairs to join our team. This role will develop, propose and implement well-informed global regulatory strategies within a highly cross-functional, collaborative, project team environment. The Senior Manager will provide regulatory support 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 ...Read more about Senior Manager, Regulatory Affairs (Clinical)More
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Vancouver, BC, Canada ● Req #315Tuesday, January 14, 2025We are seeking a Senior Director/Executive Director, Program Management, CMC to join our team. Working in close collaboration with both cross-functional program teams, with emphasis on CMC and Regulatory functions, the incumbent will lead the translation of CMC program strategies into concrete deliverables and integrated timelines, maintain and communicate key project documents (project plans, risk registers, action items, etc.), and provide team support through validation and commercial launch ...Read more about Senior Director/Executive Director, Program Management, CMCMore
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Boston, MA, USA ● Req #315Tuesday, January 14, 2025We are seeking a Senior Director/Executive Director, Program Management, CMC to join our team. Working in close collaboration with both cross-functional program teams, with emphasis on CMC and Regulatory functions, the incumbent will lead the translation of CMC program strategies into concrete deliverables and integrated timelines, maintain and communicate key project documents (project plans, risk registers, action items, etc.), and provide team support through validation and commercial launch ...Read more about Senior Director/Executive Director, Program Management, CMCMore
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We are seeking an Executive Assistant/Office Manager to join our team. This pivotal role provides high-level administrative support to the CEO, CFO, and EVP, Strategy & Innovation, ensuring seamless calendar management, travel coordination, and meeting logistics. The Executive Assistant/Office Manager will also support investor relations activities, including scheduling meetings, managing IR data, and organizing conferences and other IR events. Additionally, as Office Manager for our Vancouver ...Read more about Executive Assistant/Office ManagerMore
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Boston, MA, USA ● Req #303Wednesday, December 18, 2024We are seeking a Senior Director/Executive Director, Development Program Management to co-lead and manage cross-functional planning of Xenon’s small-molecule early stage Development Track Candidate (DTC) programs advancing to IND and beyond. This position would partner with the Product Development Team Leader (PDTL) and Product Development Team (PDT) to lead the strategic planning and execution of multiple DTC candidates. Prior experience advancing drug candidates to IND and beyond is required ...Read more about Senior Director/Executive Director, Development Program ManagementMore
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We are seeking a 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 Director will collaborate with IT business partners and colleagues in key functions to ...Read more about Director, Data Architecture & EngineeringMore
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Vancouver, BC, Canada ● Req #272Tuesday, May 14, 2024We are seeking an Associate Director/Director, Clinical Programming & Data Standards to join our team. This role will provide expert-level hands-on principal programming support and technical leadership to develop, maintain, validate, and run SAS computer programs that access, visualize, and report clinical trial data, in accordance with various clinical plans, ICH guidelines, and applicable regulatory requirements. As an Associate Director/Director of Clinical Programing and Data Standards, you ...Read more about Associate Director/Director, Clinical Programming & Data StandardsMore
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Boston, MA, USA ● Req #272Tuesday, May 14, 2024We are seeking an Associate Director/Director, Clinical Programming & Data Standards to join our team. This role will provide expert-level hands-on principal programming support and technical leadership to develop, maintain, validate, and run SAS computer programs that access, visualize, and report clinical trial data, in accordance with various clinical plans, ICH guidelines, and applicable regulatory requirements. As an Associate Director/Director of Clinical Programing and Data Standards, you ...Read more about Associate Director/Director, Clinical Programming & Data StandardsMore