3 дня назад
Senior Director, Global Medical Expert - Gene Therapies (Gene Therapies)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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