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8 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 medicines and drug development): Driving cross-functional clinical-stage oncology programs from preclinical development through licensure and lifecycle management with an accent on program strategy, timelines, budgets, and governance communication. Focus on coordinating Phase 1–3 development, resolving complex program risks, and enabling decisions across scientific and functional teams.

Location: Cambridge, Massachusetts, United States; 70% in-office work model. Due to U.S. export control requirements, only U.S. persons are eligible. Visa sponsorship for non-U.S. persons is not available.

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

Company

hirify.global develops mRNA medicines and operates a technology platform focused on transforming how medicines are created and delivered.

What you will do

  • Partner with program leadership to shape strategy and execution plans for oncology programs.
  • Coordinate cross-functional teams across preclinical and clinical drug development.
  • Identify, escalate, and resolve program risks and challenges through scenario planning.
  • Track program timelines, budgets, activities, risks, and decision-enabling materials.
  • Facilitate meetings, drive decision-making, document actions, and communicate status to governance bodies and executive leadership.
  • Support the development and scaling of program management capabilities, tools, and processes.

Requirements

  • BS degree in a scientific field and at least 10 years of experience, or MS degree in a scientific field and at least 8 years of experience in biotechnology or pharmaceuticals.
  • Successful project management experience in drug development across preclinical and Phase 1–3 clinical development, preferably in oncology.
  • Experience working with cross-functional teams with timeline and budget responsibility.
  • Knowledge of 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.

Nice to have

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

Culture & Benefits

  • 70/30 work model emphasizing in-office collaboration, teamwork, and mentorship.
  • Healthcare and voluntary benefits.
  • Fitness, mindfulness, and mental health resources.
  • Family planning, fertility, adoption, and surrogacy support.
  • Paid time off, volunteer days, sabbatical, global recharge days, and year-end shutdown.
  • Savings and investment programs.

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