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Senior Director, Medical Affairs (Medical Devices)

250 000 - 300 000$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Релокация
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 Director, Medical Affairs (Medical Devices): Leading clinical trials and pharmacovigilance across North America with an accent on clinical evidence generation, safety oversight, and regulatory compliance. Focus on directing cross-functional medical strategy, managing adverse event reporting decisions, and developing leaders and long-range priorities in a global matrixed organization.

Location: Center Valley, Pennsylvania, United States; hybrid with onsite presence required at least three days per week. Preference for candidates in the Northeast or East Coast; relocation assistance within the continental US is available. Up to 30% domestic travel.

Salary: $250,000–$300,000 per year.

Company

hirify.global develops, manufactures, and markets medical products and services, including infusion therapy, pain management, nutrition, pharmacy compounding, ostomy and wound care, and dialysis solutions.

What you will do

  • Lead Clinical Trials and Pharmacovigilance teams across the United States and Canada.
  • Develop clinical study plans and publication strategies for new and existing products.
  • Serve as Local Safety Officer, overseeing adverse event assessments and regulatory reporting decisions.
  • Ensure compliance with Good Clinical Practice, regulatory requirements, and company policies.
  • Partner with R&D, Regulatory, Commercial, Product Development, and Global Medical Affairs teams on clinical evidence and product lifecycle strategy.
  • Manage budgets, resources, strategic priorities, and leadership development across the department.

Requirements

  • MD, PharmD, or PhD required.
  • 10–15 years of experience in Medical Affairs, Clinical Development, Pharmacovigilance, or related life sciences functions.
  • At least five years of leadership experience managing teams and leaders.
  • Experience generating pre-market and post-market clinical evidence, preferably for medical devices or combination products.
  • Strong knowledge of clinical research, regulatory requirements, and drug/device safety.
  • Experience leading in a matrixed, global organization, with strong communication, decision-making, and stakeholder-influence skills.

Culture & Benefits

  • Highly collaborative, fast-paced environment with interaction across global teams and senior leadership.
  • Healthcare benefits and a 401(k) plan.
  • Tuition reimbursement.
  • Culture focused on knowledge sharing, continuous improvement, efficiency, sustainability, and patient safety.

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