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Boston, MA, USA ● Req #268Monday, October 7, 2024We are seeking a Senior Medical Director, Pharmacovigilance and Drug Safety (DSPV) to join our team. The Senior Medical Director, DSPV 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 p ...Read more about Senior Medical Director, Pharmacovigilance and Drug SafetyMore
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We are seeking a Manager or 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 a ...Read more about Manager/Senior Manager, Trial OperationsMore
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We are seeking a Vice President, Early Clinical Development to join our team. The Vice President will lead all early development programs from drug candidate selection through to Phase 2 proof of concept. In addition, the Vice President will build the early development department including the pharmacology function to enable the design and efficient execution of all early development programs across multiple therapeutic areas including, epilepsy, psychiatry, and pain. Responsibilities will inclu ...Read more about Vice President, Early Clinical DevelopmentMore
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We are seeking a Human Resources Coordinator/Senior Human Resources Coordinator to join the HR Operations team on a 12-month contract. The Human Resources Coordinator/Sr. Human Resources Coordinator is responsible for ensuring the entering and coordination of data, documents and processes into the various HR systems in an accurate and timely manner to ensure flawless execution. As a representative of the HR team, the successful candidate will work to ensure the department and company processes a ...Read more about HR Coordinator/Senior HR CoordinatorMore
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We are seeking a Manager or 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 a ...Read more about Manager/Senior Manager, Trial OperationsMore
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We are seeking a Senior Administrator, Human Resources to join our Human Resources team. The Senior Administrator will be responsible for coordinating recruitment scheduling for executive level positions (VP and above), scheduling Senior Hire orientations and supporting training events for department heads, supporting contracts and Statements of Work along with department budget tracking and reconciliations, providing administrative support for the Executive Vice President, Human Resources and o ...Read more about Senior Administrator, Human ResourcesMore
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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 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 stu ...Read more about Senior Manager, Regulatory Affairs (Clinical)More
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Boston, MA, USA ● Req #305Thursday, August 15, 2024We are seeking a Senior Manager/Associate Director, Supply Chain Planning to join our team. The Senior Manager/Associate Director, Supply Chain Planning will be responsible for supply chain planning for clinical supplies (clinical trial material) across a number of small molecule drug development programs in support of Xenon’s clinical trials. The Senior Manager, Supply Chain Planning will additionally be responsible for developing and managing end-to-end supply chain plans for Xenon’s products ...Read more about Senior Manager/Associate Director, Supply Chain PlanningMore
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We are seeking a Medical Editor 2/Senior Medical Editor to join our team and help us deliver top-quality regulatory documents. The ideal candidate will be responsible for reviewing and editing regulatory documents for accuracy and clarity, as well as ensuring that the content meets our in house style guidelines and standards. The editor will ensure that facts, data, and scientific units have been used accurately and consistently. The editor will query potential problems with logic, organization, ...Read more about Medical Editor 2/Senior Medical EditorMore
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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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Boston, MA, USA ● Req #256Wednesday, August 14, 2024We are seeking a Director, Manufacturing, Quality & Supply Chain (MQ&SC) Information Systems, to join our team. This role will be the IT business partner for the drug substance and drug product teams (note that Xenon does not have – or intend to have – internal manufacturing facilities); the Quality organization; the supply chain function; and the development program management team. The Director will be the primary point of contact on all topics related to IT. The Director will partner with th ...Read more about Director, Manufacturing, Quality & Supply Chain Information SystemsMore
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Boston, MA, USA ● Req #303Tuesday, August 13, 2024We are seeking an Associate Director/Director, Development Program Management to join our team. The Associate Director/Director, Development Program Management will 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 (e.g. INDs, NDAs, MAAs) and life cycle management projects. This role involves close coordination with stakeholders within development (e.g., Clinical De ...Read more about Associate Director/Director, Development Program ManagementMore
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We are seeking a Senior Scientist, CMC, Drug Product to join our team. The candidate will be responsible for leading the development of suitable formulations for the in vivo assessment (including for GLP toxicology studies) of novel chemical compounds originating from our Discovery team. Additionally, the incumbent will support the physicochemical characterization of compounds that are deemed to be of interest for further downstream clinical development. This is a hands-on, laboratory-based posi ...Read more about Senior Scientist, CMC, Drug ProductMore
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Boston, MA, USA ● Req #297Thursday, August 1, 2024We are seeking an Executive Medical Director, Pharmacovigilance and Drug Safety (DSPV), to join our team. The Executive Medical Director, DSPV will play a key leadership role in Drug Safety Pharmacovigilance, building Medical Safety and Risk Management team, supervising and mentoring safety physicians and safety scientists, responsible for safety and benefit-risk assessment of all Xenon’s products throughout the product lifecycle (from First-In-Human to post-marketing), providing strategic leade ...Read more about Executive Medical Director, Pharmacovigilance and Drug SafetyMore
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We are seeking a Senior Manager, CMC, Quality Control to join our team. The Senior Manager, CMC, Quality Control will work flexibly across several small molecule drug development programs with an emphasis on managing outsourced testing and stability program for the cGMP API and drug product (DP) manufacturing and testing campaigns. This position reports to the Associate Director, CMC, Quality Control and will be in Vancouver, BC, Canada. We will consider other jurisdictions for exceptional candi ...Read more about Senior Manager, CMC, Quality ControlMore
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Boston, MA, USA ● Req #259Friday, July 12, 2024We are seeking a Director, Pharmacovigilance and Drug Safety (Safety Science) 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 Directo demonstrates effective prioritization, critical thinking and judgment-based d ...Read more about Director, Pharmacovigilance and Drug Safety (Safety Science)More
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We are seeking a Clinical Scientist 1 or 2 to join our team. The Clinical Scientist 1 or 2 will be a member of a highly collaborative Clinical Development team, with involvement in a diverse range of activities. This position reports to the Vice President, Clinical Development and will be in Boston, MA, USA. This role is a hybrid position, requiring a minimum of 2 days per week in the office. The level of the position will be commensurate with the candidate’s education and industry experience. R ...Read more about Clinical Scientist 1 or 2More
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We are seeking a Clinical Scientist 1 or 2 to join our team. The Clinical Scientist 1 or 2 will be a member of a highly collaborative Clinical Development team, with involvement in a diverse range of activities. This position reports to the Vice President, Clinical Development and will be in Vancouver, BC, Canada. This role is a hybrid position, requiring a minimum of 2 days per week in the office. The level of the position will be commensurate with the candidate’s education and industry experie ...Read more about Clinical Scientist 1 or 2More
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We are seeking a Director, Scientific Communications to join our team. The Director, Scientific Communications is responsible for developing and managing the strategic planning and execution of scientific communications tactics, including publication plans, medical communications initiatives, and scientific training materials. This individual provides oversight and assistance to Medical Affairs, internal partners, and external vendors to ensure completion of scientific communications projects in ...Read more about Director, Scientific Communications (Publications)More
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We are seeking an Associate Director/Director, Human Resources to join our team. The Associate Director/Director, Human Resources will bring life sciences industry expertise to manage the Compensation program (non-executive, commercial) in support of Xenon’s compensation philosophy to continue strong talent attraction and retention, and act as a Business Partner providing counsel, coaching and support to assigned departments, employees and managers in the U.S. and Canada. The Associate Directo ...Read more about Associate Director/Director, Human ResourcesMore
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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
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Boston, MA, USA ● Req #265Sunday, May 5, 2024We are seeking a Director, Pharmacovigilance and Drug Safety (Operations & Compliance) to join our team. This important leadership role in the Pharmacovigilance Operations & Compliance team will be responsible for the establishment, maintenance and oversight of appropriate procedures and systems to assure adherence to local and international regulatory requirements for collection, processing, and reporting of safety information throughout the product life cycle. They may be deployed to one or m ...Read more about Director, Pharmacovigilance and Drug Safety (Operations & Compliance)More
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Boston, MA, USA ● Req #235Thursday, March 7, 2024We 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 Affairs (Medical and Scientific Ops)More