Company Description
Xenon Pharmaceuticals Inc. (NASDAQ: XENE) is a neuroscience-focused biopharmaceutical company dedicated to discovering, developing, and commercializing innovative therapeutics to improve the lives of individuals with neurological and psychiatric disorders. We are seeking individuals who thrive in a respectful, collaborative, and inclusive culture to join our team. Our product pipeline addresses high unmet medical needs, including epilepsy and depression. Our leading program, azetukalner, is the most advanced potassium channel modulator in clinical development for multiple indications, with ongoing and planned Phase 3 clinical trials. With strong discovery, clinical development, and commercial operations, backed by a solid balance sheet, Xenon continues to grow as a premier neuroscience company.
Role Description
This is a full-time on-site role as Executive Director, Medical Affairs located in Greater Boston. The Executive Director, Medical Affairs will be responsible for developing and executing medical strategies to support the clinical development and commercialization of our products. This includes leading medical communication efforts, engaging with key opinion leaders, overseeing clinical research activities, and providing medical expertise to various internal departments. The role requires significant cross-functional collaboration with clinical development, regulatory affairs, marketing, and commercial teams to ensure the alignment of medical strategies with corporate goals.
Qualifications
- Extensive experience in medical affairs, clinical research, or related fields within a biopharmaceutical company
- Strong expertise in neuroscience, with a focus on neurological and psychiatric disorders
- Excellent leadership and project management skills
- Proven ability to build relationships with key opinion leaders and stakeholders
- Exceptional written and verbal communication skills, including medical writing and presentation abilities
- MD, PhD, or PharmD degree in a relevant scientific discipline
- Ability to work effectively on-site in Greater Boston
- Knowledge of regulatory requirements and experience with regulatory submissions
