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3 дня назад

Clinical Science Director (Oncology)

195 000 - 277 500$
Формат работы
remote (только USA)/onsite
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
Clinical Science Director (Oncology) (clinical development): Designing and developing early- and late-phase oncology studies with an accent on clinical trial protocols, investigator collaboration, safety analysis, and regulatory documentation. Focus on interpreting clinical data, preparing scientific publications and health-authority reports, and coordinating complex studies involving targeted and immunological therapies.

Location: Alameda, California, United States, with remote work available from the United States; 10–25% travel required.

Base salary: $195,000–$277,500 annually, depending on geographic market, knowledge, skills, experience, and internal equity.

Company

hirify.global is a biotechnology and pharmaceutical company developing investigational therapies, including oncology medicines.

What you will do

  • Design, plan, and initiate early- and late-phase clinical oncology studies and develop study synopses, protocols, and related documentation.
  • Collaborate with clinical operations and study teams on informed consent forms, case report forms, training materials, site visits, and investigator meetings.
  • Work with investigators and oncology thought leaders, support investigator selection, and maintain relationships throughout clinical studies.
  • Analyze and report potential safety events and contribute to clinical data interpretation, regulatory filings, and study close-out reports.
  • Write and review abstracts, publications, presentations, and scientific materials for physicians, external customers, and internal stakeholders.
  • Provide clinical education and feedback on emerging clinical and competitive trends in oncology.

Requirements

  • Pharm.D., PhD, or M.D. with at least 8 years of related experience, or an equivalent combination of education and experience.
  • 5–8 years of clinical development experience in biotechnology, pharmaceuticals, academia, or a combination of these environments.
  • Experience participating in clinical oncology studies involving molecular targeted or immunological therapies.
  • Detailed knowledge of clinical trial implementation and the drug development process, including the design, execution, and reporting of oncology trials with small- and large-molecule candidates.
  • Strong analytical, business communication, public speaking, presentation, organizational, and problem-solving skills.
  • Ability to work under tight timelines and apply sound judgment to complex clinical and scientific problems.

Culture & Benefits

  • Collaborative office environment focused on sharing ideas and solutions.
  • Comprehensive employee benefits, including medical, dental, vision, life, disability, and flexible spending account coverage.
  • 401(k) plan with company contributions and eligibility for a discretionary annual bonus and long-term incentives.
  • 15 vacation days in the first year, 17 paid holidays including a company-wide winter shutdown, and up to 10 sick days annually.
  • Company-provided equipment, including dual monitors and ergonomic chairs.

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