X

Xenon Pharmaceuticals

Clinical-stage neurological disorder therapeutics developer

Vice President, Clinical Development - Pain

Biology & BiotechConfirmed live in the last 24 hours
Full-timeBoston, MA, USA

About the Job

Requirements

  • An MD and experience in pain drug development are required.
  • At least 12 years of clinical experience in a pharmaceutical or biotechnology environment are required.
  • At least 5 years of experience as a drug development program lead and/or managing teams are required.
  • Experience filing Investigational New Drug applications and New Drug Applications, and bringing novel therapeutics into clinical development, is required.
  • Experience designing and executing pain clinical trials to demonstrate safety and efficacy is required.
  • Broad experience implementing and executing Phase 1–3 clinical trial designs and interpreting clinical data is required.
  • Training in Good Clinical Practice and knowledge of the research process, protocol adherence, and accurate collection and documentation of research data are required.
  • Understanding of clinical trial operations, biostatistics, and data management techniques is required.
  • A good understanding of clinical pharmacology principles is required.
  • Working knowledge of health authority regulations regarding evaluation and approval processes is required.
  • Scientific acumen and leadership skills sufficient to establish credibility and confidence within and outside the company are required.
  • The ability to contribute as both a leader and a member of a small team is required.
  • Adherence to high ethical standards is required.
  • Strong written and verbal communication skills are required.
  • Creative problem-solving skills, flexibility of thought, openness to new ideas, and the ability to motivate and maintain a positive work environment are required.
  • Strong team organization and delegation skills, the ability to promote cooperation among staff, and the ability to resolve conflicts constructively are required.
  • Willingness to travel domestically and internationally up to 30% of the time is required.

Responsibilities

  • Develop and propose clinical development strategies for all pain development programs in compliance with global regulatory standards and in collaboration with key functional areas, external vendors, and advisors.
  • Collaborate with Program Management to run efficient and productive drug development program teams across all pain drug development programs.
  • Provide scientific and drug development expertise to the cross-functional development team through reviews of scientific literature and indication knowledge.
  • Monitor external research and regulatory environments and emerging study data to ensure clinical development plans remain appropriate.
  • Identify and build relationships with key opinion leaders to promote scientific discussions in accordance with engagement strategies and plans.
  • Assemble expert panels and lead the management and hosting of advisory boards and other scientific consultant meetings to advise on clinical development.
  • Establish and manage Data Monitoring Safety Boards as needed in collaboration with Drug Safety and Pharmacovigilance.
  • Oversee analysis of potential safety events within and across studies in collaboration with Drug Safety and Pharmacovigilance.
  • Participate in reviewing and interpreting clinical trial data and provide insight into the clinical relevance of trial results.
  • Provide scientific input to regulatory documents for submissions and discussions with health authorities.
  • Contribute to publication plans and clinical data communications in collaboration with Medical Affairs.
  • Present program strategic plans to the Executive Leadership Team and Board of Directors as programs progress.
  • Develop short- and long-term functional objectives in accordance with company strategies and plans.
  • Plan and manage budget proposals and approved budgets in accordance with company strategic and operating plans and Finance policies.
  • Recruit, lead, direct, develop, coach, and evaluate direct reports, if any, in accordance with company human resources policies and practices.
  • Act in accordance with company policies, including the Code of Business Conduct and Ethics, and ensure direct reports understand and follow policies.
  • Perform other duties as assigned.

About the Company

Xenon Pharmaceuticals

Clinical-stage neurological disorder therapeutics developer

Xenon Pharmaceuticals is a clinical-stage biopharmaceutical company focused on developing therapies for neurological disorders, especially epilepsy, through research and collaboration with partners and licensors to support eventual product commercialization. Its drug candidates are designed to treat CNS and genetic contributors to disease, with examples like XEN007 reaching Phase 2 proof-of-concept in treatment-resistant pediatric childhood absence epilepsy, illustrating targeted therapeutic development. The company concentrates on genetics-informed neurology and maintains a pipeline funded in part by partnerships and licensing, setting it apart from broader pharma players. Its goal is to discover, develop, and bring therapies to patients to address unmet needs in neurology and epilepsy.

Company size
201-500
Company stage
IPO
Headquarters
Burnaby, Canada
Founded
1996

Recently Posted Jobs

Explore more opportunities at Xenon Pharmaceuticals

See more jobs