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3 дня назад

Senior Director, Global Medical Expert - Gene Therapies (Gene Therapies)

Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
UK/Switzerland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Director, Global Medical Expert - Gene Therapies (Gene Therapies): Leading medical affairs implementation of one-time gene therapies for rare diseases across EMEA with an accent on treating-site onboarding, scientific education, and patient management. Focus on developing treatment-center training, guiding post-approval activities, supporting regulatory submissions and evidence generation, and coordinating cross-functional medical strategy.

Location: London, England or Zurich, Switzerland; hybrid work with onsite attendance typically required 2–3 days per week or more depending on business needs. Travel is estimated at 25%–35%.

Company

hirify.global is a biopharmaceutical company developing innovative medicines for rare diseases and gene therapy.

What you will do

  • Lead compliant scientific discussions with treating physicians and external medical experts across EMEA.
  • Enable implementation of gene therapies through pre-approval managed access programs and post-approval commercial treatment.
  • Develop educational materials and training for gene therapy treatment centers, covering safety, efficacy, patient management, immunomodulation, and outcomes.
  • Respond to treating-site inquiries and support country-level regulatory submissions and data-generation initiatives.
  • Advise on publications and medical materials, address evidence gaps, and support clinical decision-making.
  • Partner with global and regional medical affairs, clinical development, safety, CMC, and commercial teams on gene therapy strategy and launches.

Requirements

  • Medical Doctor, MBBS, or equivalent; a PhD is preferred.
  • Subspecialty training and certification in Clinical Immunology, Clinical or Biochemical Genetics, Rheumatology, or Neurology.
  • At least 5 years of academic or faculty experience with a strong publication record.
  • At least 3 years of pharmaceutical experience in drug development, clinical trials, or Medical Affairs.
  • Direct experience managing patients receiving systemic AAV gene therapy in clinical trials or after regulatory approval.
  • Ability to lead complex post-approval activities, make strategic medical decisions, and work effectively in cross-functional and multidisciplinary environments.

Nice to have

  • PhD qualification.
  • Established network of experts and leaders in the rare disease community.

Culture & Benefits

  • Supportive and inclusive environment focused on learning and professional growth.
  • Generous vacation time and company-observed public holidays.
  • Volunteer days, wellbeing benefits, and fitness reimbursement.
  • Long-term incentive and employee stock purchase plans or equivalent offerings.
  • Tuition sponsorship and professional development plans, with benefits varying by region and country.

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