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6 дней назад

Director, Program Management, Oncology

167 000 - 300 700$
Формат работы
hybrid
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
Director, Program Management, Oncology (mRNA/Drug Development): Driving cross-functional clinical-stage oncology programs from preclinical development through licensure and lifecycle management with an accent on program strategy, timeline and budget control, and executive governance. Focus on scenario planning, resolving cross-functional development challenges, and enabling decisions across Phase 1–3 drug development.

Location: Cambridge, Massachusetts, United States; 70% in-office hybrid work model. Only U.S. persons are eligible due to export control requirements.

Salary: $167,000–$300,700 per year, with potential discretionary bonus, incentive compensation, or equity.

Company

hirify.global develops mRNA-based medicines and vaccines across oncology, infectious diseases, rare diseases, and cardiovascular diseases.

What you will do

  • Partner with program leaders to shape strategy and execution plans for 1–3 clinical-stage oncology programs.
  • Coordinate cross-functional teams across preclinical and clinical development, including Phase 1–3 activities.
  • Identify, escalate, and resolve program risks and challenges through scenario planning and structured decision-making.
  • Track program timelines, budgets, activities, risks, and status for governance bodies and executive leadership.
  • Facilitate cross-functional meetings, prepare agendas and minutes, and manage action items.
  • Contribute to the development and scaling of program management capabilities, tools, and processes.

Requirements

  • BS in a scientific field with at least 10 years of experience, or MS in a scientific field with at least 8 years of experience in biotechnology or pharmaceuticals.
  • Successful project management experience in drug development across multiple preclinical and clinical phases, preferably in oncology.
  • Experience working with cross-functional teams and responsibility for timelines and budgets.
  • Proficiency with project management tools such as Smartsheet, MS Project, and timeline visualization software.
  • Strong communication, organization, influencing, conflict management, and collaboration skills.
  • Must qualify as a U.S. person under U.S. export control laws; visa sponsorship for non-U.S. persons is not available.

Nice to have

  • Project or program management training.
  • Ph.D. or PharmD.
  • Oncology program management experience.

Culture & Benefits

  • 70/30 hybrid model emphasizing in-office collaboration, innovation, teamwork, and mentorship.
  • Competitive healthcare and voluntary benefit programs.
  • Fitness, mindfulness, mental health, family planning, fertility, adoption, and surrogacy support.
  • Paid vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown.
  • Savings and investment programs, plus location-specific perks.

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