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9 часов назад

Director/Sr. Director Program Management (Biotech)

231 000 - 319 000$
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/Sr. Director Program Management (Biotech): Managing integrated development programs for allogeneic gamma delta T cell therapies with an accent on cross-functional planning, milestone tracking, risk management, and resource coordination. Focus on building program timelines, resolving execution challenges, facilitating governance, and communicating program status across pharmaceutical and biotech functions.

Location: Redwood City, California, United States; onsite at least three days per week, with Tuesday–Thursday mandatory. Some roles may require full-time onsite presence.

Salary: $231,000–$319,000 USD per year, plus annual cash bonus and long-term equity incentives.

Company

hirify.global is a clinical-stage biotechnology company developing allogeneic gamma delta T cell therapies for autoimmune diseases and cancer.

What you will do

  • Create and maintain integrated program timelines, Gantt charts, dependencies, milestones, and critical-path activities.
  • Coordinate cross-functional planning and execution in alignment with product development plans and budgets.
  • Facilitate program team, governance, and team-building meetings; document decisions, meeting minutes, and action items.
  • Identify program risks, resource constraints, and execution challenges, and drive mitigation and resolution.
  • Prepare program status reports covering milestones, issues, decisions, and progress for senior management.
  • Support budget tracking, documentation platforms, lessons-learned sessions, and continuous improvement of program management tools and processes.

Requirements

  • BA/BS degree required; an advanced degree such as PharmD or PhD is highly desirable.
  • 10+ years of industry experience, including at least 5 years of project management experience in cross-functional pharmaceutical or biotech teams.
  • Deep understanding of the drug development process and demonstrated ability to manage plans and timelines across multiple functional areas.
  • Strong planning, organizational, analytical, communication, leadership, facilitation, negotiation, and influence-management skills.
  • Experience with established project management tools such as MS Project or Smartsheet.
  • Ability to work independently, resolve program obstacles, build trust, and collaborate effectively in a matrix environment.

Nice to have

  • Experience in oncology or autoimmune diseases.
  • Cell therapy experience.
  • PMP certification.
  • Experience managing junior program management staff.

Culture & Benefits

  • Collaborative, high-performing environment prioritizing in-person engagement.
  • Competitive compensation with annual bonus, equity incentives, ESPP, and a 401(k) with Roth option and 4.5% company match.
  • Medical, dental, vision, FSA, HSA matching, life, disability, legal, pet, and other insurance programs.
  • Paid time off including company holidays, winter break, vacation, sick time, and parental leave.
  • State-of-the-art facility with onsite gym, parking and EV charging, Caltrain shuttle, subsidized lunches, and stocked breakrooms.

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