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10 дней назад

Associate Director, Lymphoma, U.S. Medical Affairs

177 905 - 230 230$
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
Associate Director, Lymphoma, U.S. Medical Affairs (Oncology): Leading U.S. medical strategy and cross-functional execution for lymphoma therapies, including scientific exchange, evidence generation, and medical content development with an accent on oncology, cell therapy, and compliant Medical Affairs processes. Focus on translating clinical data into actionable strategy, coordinating advisory boards and publications, and managing complex initiatives across Field Medical, Commercial, HEOR/RWE, Clinical Development, Regulatory, and Global Medical Affairs.

Location: United States — El Segundo, CA; Foster City, CA; Thousand Oaks, CA; or Parsippany, NJ. The role includes approximately 35% domestic and international travel.

Salary: $177,905–$230,230 for other U.S. locations; $195,670–$253,220 for the Bay Area, plus potential bonus, long-term incentives, paid time off, and benefits.

Company

hirify.global is a biopharmaceutical company developing CAR T-cell and T-cell receptor engineered therapies for cancer treatment.

What you will do

  • Lead priority workstreams supporting the U.S. lymphoma Medical Affairs strategy.
  • Partner with Field Medical, Commercial, Market Access, HEOR/RWE, Clinical Development, Regulatory, Safety, and Global Medical Affairs.
  • Translate clinical data, disease-area insights, and stakeholder perspectives into medical strategy, field priorities, and evidence-generation opportunities.
  • Develop scientific communication platforms, medical content, FAQs, presentations, and field resources.
  • Co-lead advisory boards, congress activities, symposia, medical education initiatives, and expert engagement plans.
  • Manage cross-functional teams, timelines, budgets, deliverables, agency partners, publications, and real-world evidence initiatives.

Requirements

  • Advanced scientific or medical degree required; MD, PharmD, PhD, or equivalent degree in life sciences, immunology, oncology, or a related discipline preferred.
  • BA/BS with 10 years of relevant experience, MA/MS with 8 years, or PhD/PharmD with 2 years of relevant experience.
  • At least 5 years of pharmaceutical or biotechnology experience, including Medical Affairs experience in oncology.
  • Experience in lymphoma, leukemia, or cell therapy is strongly preferred.
  • Strong knowledge of Medical Affairs strategy, evidence generation, scientific exchange, publication planning, and compliant medical review.
  • Strong communication, project management, analytical, prioritization, and cross-functional collaboration skills; proficiency with Microsoft Word, PowerPoint, Excel, and project management tools.

Nice to have

  • Experience with lymphoma, leukemia, or engineered cell therapies.
  • Experience partnering with external experts and leading initiatives in a matrixed environment.

Culture & Benefits

  • Work within a mission focused on developing innovative cancer immunotherapies and improving patient outcomes.
  • Collaborative environment spanning medical, scientific, commercial, clinical, regulatory, and operational functions.
  • Benefits include company-sponsored medical, dental, vision, and life insurance plans.
  • Paid time off, potential annual bonus, and discretionary stock-based long-term incentives may be available.

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