Назад
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2 часа назад

Executive Medical Director, Clinical Program Lead, Immunology / Rheumatology

390 000 - 527 600$
Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
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
Executive Medical Director, Clinical Program Lead, Immunology / Rheumatology (Clinical Development): Providing clinical scientific leadership for a non-I/O BCMA cell therapy program and directing clinical development strategy and trial execution with an accent on innovative FIH and Phase 2/3 program design. Focus on leading multidisciplinary teams, managing IND and BLA/NDA development activities, and guiding study execution, medical review, database locks, and health authority responses.

Location: Tarrytown, New York or Warren, New Jersey, United States. The role includes approximately 10% travel to relevant conferences and congresses.

Salary: $390,000–$527,600 annually

Company

Regeneron develops medicines for people with serious diseases through science and innovation.

What you will do

  • Provide overall clinical scientific leadership for the non-I/O BCMA program within Hematology.
  • Develop clinical development strategy and execute clinical trials in partnership with the Global Program Head.
  • Act as a medical expert in interactions with regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups, and internal functions.
  • Design innovative first-in-human and Phase 2/3 programs that support efficient development in an evolving regulatory environment.
  • Lead multidisciplinary, matrixed clinical teams and build consensus around data-driven decisions.
  • Lead and develop a team of MDs and clinical scientists.

Requirements

  • Advanced medical degree, MD or equivalent, is required.
  • 6–8 years of industry experience in related therapeutic-area clinical development is preferred.
  • Leadership experience working with senior clinical development staff and external collaborators, including opinion leaders and regulators.
  • Substantial drug development experience, including both IND and BLA/NDA submissions.
  • Experience with study start-up, study team execution, data cleaning, medical review, database locks, and health authority responses.
  • Strong commitment to improving patient outcomes through drug development and ability to work effectively in a team setting.

Nice to have

  • Specialized fellowship training in Immunology or Rheumatology.
  • People management experience.

Culture & Benefits

  • Inclusive workplace culture and equal employment opportunity.
  • Competitive total rewards package that may include annual bonuses, equity awards, retirement benefits, health and wellness programs, insurance, paid time off, and family support benefits.
  • Many roles are expected to be performed onsite because work is considered most effective when employees are together.
  • Background checks may verify identity, right to work, and educational qualifications where required by local law.

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