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3 дня назад

Senior Director, Clinical Operations (Biotech, Oncology)

246 000 - 349 500$
Формат работы
onsite
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
Senior Director, Clinical Operations (Biotech, Oncology) (Oncology clinical trials and biotech): Leading worldwide execution of Phase I–IV oncology clinical programs and developing operational strategies, delivery plans, budgets, and resource models with an accent on clinical development planning, CRO oversight, and regulatory compliance. Focus on managing complex cross-functional programs, solving operational delivery challenges, and leading Clinical Operations teams through strategic change and innovation.

Location: Alameda, California, United States; travel required up to 20%

Salary: $246,000–$349,500 annually, plus potential annual bonus and long-term incentives

Company

hirify.global is a biotechnology company developing and commercializing oncology products through global clinical development programs.

What you will do

  • Lead worldwide operational execution of Phase I–IV oncology clinical trials across assigned programs.
  • Develop operational strategies, delivery plans, Clinical Development Plan inputs, protocols, timelines, budgets, and resource models.
  • Represent Clinical Operations on Product Development Teams, Clinical Sub-teams, governance boards, and external strategy teams.
  • Oversee CROs, vendors, Study Delivery Leads, and Indication Leads to manage risks, quality, inspection readiness, and delivery against plan.
  • Partner with Clinical Development, Regulatory Affairs, Clinical Pharmacology, Statistics, Medical Affairs, Data Management, and Medical Writing.
  • Lead and mentor Clinical Operations employees while driving process improvement, innovation, change management, and standardization.

Requirements

  • Must work from the Alameda, California location.
  • Bachelor’s degree with at least 15 years of related experience, master’s degree with at least 13 years, PhD with at least 12 years, or an equivalent combination; typically 18 years of related experience is required.
  • Extensive clinical operations experience in the pharmaceutical, biotechnology, or CRO environment, including oncology program delivery.
  • Experience managing outsourced studies and working with Contract Research Organizations, investigators, external experts, and vendors.
  • Expertise in clinical development, study protocols, study management, timelines, budgets, regulatory guidelines, and inspection readiness.
  • Strong leadership, strategic thinking, financial management, negotiation, influencing, stakeholder management, and communication skills.

Nice to have

  • Experience in the biotech or pharmaceutical industry.
  • Knowledge of scientific and medical literature in oncology.
  • Experience representing Clinical Operations at congresses, industry bodies, or other external opportunities.

Culture & Benefits

  • Collaborative office environment designed to support teamwork, idea sharing, and creativity.
  • Comprehensive medical, dental, vision, life, disability, and flexible spending account benefits.
  • 401(k) plan with company contributions, stock purchase opportunities, and long-term incentives.
  • 15 accrued vacation days in the first year, 17 paid holidays, a company-wide winter shutdown, and up to 10 sick days annually.
  • Equipment including dual monitors and ergonomic chairs is provided.

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