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  • Boston, MA, USA ● Req #235
    Friday, March 8, 2024
    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 ... More
  • Boston, MA, USA ● Req #233
    Friday, March 8, 2024
    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 ... More
  • Vancouver, BC, Canada ● Req #230
    Friday, March 8, 2024
    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 ... More
  • Boston, MA, USA ● Req #229
    Friday, March 8, 2024
    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 ... More
  • Boston, MA, USA ● Req #227
    Friday, March 8, 2024
    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 ... More
  • Vancouver, BC, Canada ● Req #226
    Friday, March 8, 2024
    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 ... More
  • Boston, MA, USA ● Req #225
    Friday, March 8, 2024
    We 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 ... More
  • Boston, MA, USA ● Req #220
    Friday, March 8, 2024
    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 ... More
  • Boston, MA, USA ● Req #208
    Friday, March 8, 2024
    We are seeking a Associate Director/Director, 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 Associate Director/Director 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 c ... More
  • Vancouver, BC, Canada ● Req #208
    Friday, March 8, 2024
    We are seeking a Associate Director/Director, 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 Associate Director/Director 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 c ... More
  • Boston, MA, USA ● Req #205
    Friday, March 8, 2024
    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 ... More
  • Boston, MA, USA ● Req #203
    Friday, March 8, 2024
    We are seeking a Senior Medical Writer to join our team. The Senior Medical Writer works flexibly across a number of preclinical and clinical stage projects, providing medical writing expertise, including data review activities. 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. RESPONSIBILITIES: Plans, writes, edits, and formats clinical development documents, in ... More
  • Boston, MA, USA ● Req #195
    Friday, March 8, 2024
    We are seeking a Director/Senior Director, Development Information Systems to join our team. This role will be the IT business partner for most of the functions reporting to the Chief Medical Officer, including Clinical Development, Clinical Operations, Translational Research, Biostatistics & Programming, and Pharmacovigilance. The Director/Senior Director, Development Information Systems will partner with those groups (+/- Regulatory Affairs, depending on the candidate’s experience and qualific ... More