Senior Director, International Regulatory Affairs

Denali Therapeutics

  • Zürich
  • Unbefristet
  • Vollzeit
  • 17 Tage her
Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.Senior Director, International Regulatory Affairs is a highly motivated and strategic regulatory professional with global expertise in drug development and regulatory submissions. This individual will be accountable for leading and executing Denali’s international regulatory strategy across a portfolio of development-stage and commercial neuroscience programs. This leader is responsible for ensuring successful interactions with Health Authorities outside the U.S., including the EMA, PMDA, and other key global agencies.
The role will oversee a team of international regulatory professionals and will partner cross-functionally to ensure regionally appropriate strategies, risk mitigation plans, and regulatory compliance. Denali is seeking candidates with a global mindset, strong technical and operational regulatory acumen, and a passion for advancing therapies that can change the lives of patients with neurodegenerative diseases.Key Accountabilities/Core Job Responsibilities:Developing and implementing international regulatory strategies for clinical development and commercial-stage products across Denali’s global portfolioLeading the planning, preparation, and submission of regulatory applications including Clinical Trial Applications (CTAs), Marketing Authorization Applications (MAAs), Orphan Drug Designations, and other key filings to Health Authorities outside the United StatesServing as the primary liaison with global Health Authorities (e.g., EMA, MHRA, PMDA, Health Canada), including leading preparation for and participation in scientific advice meetings and regulatory interactionsCollaborating with cross-functional teams to support timely initiation and maintenance of global clinical trials and product registrationsMonitoring global regulatory developments, assessing impact on programs, and translating requirements into clear regulatory strategies and recommendationsEnsuring the quality, consistency, and compliance of international regulatory submissions and communicationsLeading the development and maintenance of internal processes and tools for global regulatory activities, including policies, templates, and training initiativesPartnering with regional affiliates, CROs, and local consultants to execute submissions and maintain compliance with local requirementsSupporting global labeling strategies and alignment with U.S. labeling, where applicableMentoring, developing, and managing international regulatory team members, and fostering a culture of collaboration, innovation, and excellenceLead direct report(s) through annual goal setting, growth planning, adherence to company policies, maintain training compliance and provide ongoing feedback on growth, development and areas of improvement.Qualifications/SkillsBachelor’s degree required; advanced degree in life sciences or related discipline strongly preferred12+ years of regulatory affairs experience in the pharmaceutical or biotechnology industry, with at least 8+ years in international regulatory affairsDirect experience with major international regulatory agencies (e.g., EMA, PMDA, Health Canada, TGA, Swissmedic)Demonstrated success in leading global submissions, including CTAs and MAAs, and in developing international regulatory strategies for early- to late-stage development programsThorough knowledge of international regulatory frameworks, including ICH guidelines, EU directives, and regional requirementsStrong leadership, decision-making, and project management skills, with a demonstrated ability to drive strategic outcomes across global teamsExcellent written and verbal communication and influencing skills, including experience interacting with senior leadership and global regulatorsExperience managing and mentoring regulatory professionalsAbility to navigate complex regulatory environments with a forward-thinking, solution-oriented approachHigh level of professionalism, accountability, and commitment to ethical conductCompensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a pension, medical stipend, equity and a broad range of other benefits.Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.

Denali Therapeutics