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2 дня назад

Director/Sr. Director Program Management (Biotechnology)

231 000 - 319 000$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior/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 (Biotechnology): Driving integrated program plans, timelines, budgets, and cross-functional execution for gamma delta T cell therapies with an accent on drug development, risk management, and stakeholder alignment. Focus on maintaining critical paths, resolving program obstacles, coordinating governance, and managing resources across complex biotech programs.

Location: Redwood City, California, United States; hybrid schedule with onsite attendance at least three days per week, Tuesday–Thursday mandatory

Salary: $231,000–$319,000 USD annually

Company

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

What you will do

  • Create and maintain integrated program timelines, Gantt charts, milestones, dependencies, assumptions, and critical paths.
  • Coordinate cross-functional planning and execution in alignment with product development plans and budgets.
  • Facilitate project meetings, governance sessions, decision-making, documentation, and action-item follow-up.
  • Assess program risks, develop mitigation plans, resolve obstacles, and communicate status to stakeholders and senior management.
  • Track program budgets and resource needs in partnership with Finance and functional managers.
  • Develop project management tools and processes, support lessons learned, and may manage junior Program Management staff.

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 a cross-functional pharmaceutical or biotechnology environment.
  • Deep understanding of the drug development process and experience driving plans across multiple functional areas.
  • Strong planning, analytical, organizational, leadership, facilitation, negotiation, communication, and problem-solving skills.
  • Experience with project management planning tools such as MS Project or Smartsheet.
  • Ability to work onsite at least three days per week, with Tuesday–Thursday mandatory; some roles may require full-time onsite presence.

Nice to have

  • Experience in oncology or autoimmune diseases.
  • Cell therapy experience.
  • PMP certification.

Culture & Benefits

  • Collaborative, high-performing environment with an emphasis on in-person engagement.
  • Annual cash bonus, long-term equity incentives, Employee Stock Purchase Plan, and 401(k) with a 4.5% company match.
  • Medical, dental, vision, FSA, HSA, life, disability, legal, pet, and other insurance programs.
  • Paid holidays, winter break, vacation, sick time, and parental leave.
  • Onsite gym and fitness options, parking with electric vehicle charging, Caltrain shuttle, subsidized lunches, and stocked breakrooms.

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