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3 дня назад

Senior Scientific Director / Executive Medical Director, Medical Affairs Hematology

206 500 - 393 000$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior/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
Senior Scientific Director / Executive Medical Director, Medical Affairs Hematology (Epcoritamab and Ibrutinib): Leading medical affairs strategy, clinical data generation, scientific communications, and cross-functional programs for hematology assets with an accent on Phase II–III development, pharmacovigilance, and stakeholder engagement. Focus on designing evidence plans, guiding clinical programs, developing medical education and advisory initiatives, and coordinating global medical affairs teams.

Location: Lake County, IL preferred; Florham Park, NJ, Waltham, MA, San Francisco, CA, or Irvine, CA also considered. Hybrid schedule with office attendance Tuesday through Thursday required.

Salary: $206,500–$393,000 annual base pay, depending on job grade and other factors.

Company

hirify.global develops innovative medicines and solutions across therapeutic areas including immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Lead medical affairs strategy, functional plans, brand plans, and integrated evidence plans for Epcoritamab and Ibrutinib.
  • Collaborate with Clinical Development, Commercial, Market Access, Regulatory, HEOR, global medical teams, and affiliate functions.
  • Guide clinical data generation, Phase II–III trial design, research concepts, scientific publications, and evidence communications.
  • Lead advisory boards, medical education programs, scientific presentations, and engagement with payers, patients, prescribers, providers, and key opinion leaders.
  • Oversee medical affairs teams, cross-functional projects, governance activities, mentoring, training, budgets, timelines, and compliance.
  • Support pharmacovigilance, asset due diligence, product strategy, launches, and market access activities.

Requirements

  • For the Executive Medical Director track: M.D., D.O., or equivalent medical degree with relevant therapeutic specialty; clinical trial experience and knowledge of clinical development, regulatory requirements, and pharmacovigilance.
  • For the Senior Scientific Director track: Ph.D. or Pharm.D.; typically 15 years of pharmaceutical industry or equivalent experience, with at least 10 years in clinical trials or medical affairs.
  • Expert knowledge of the relevant therapeutic specialty and clinical trial methodology, including protocol and development strategy.
  • Proven ability to independently lead clinical programs, studies, medical affairs teams, and cross-functional teams.
  • Strong leadership, external stakeholder engagement, and strategic communication skills.
  • Excellent written and spoken English communication skills required.

Nice to have

  • Residency or fellowship completion and a national medical license.
  • Additional postdoctoral experience.
  • People management experience.
  • International experience.

Culture & Benefits

  • Collaboration across global medical, clinical, commercial, regulatory, and market access functions.
  • Paid time off, including vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) and eligibility for long-term incentive programs.
  • Opportunities to lead scientific education, research, and publication initiatives.

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