Назад
Company hidden
обновлено 16 часов назад

Clinical Science Director (Biotech Oncology)

195 000 - 277 500$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Clinical Science Director (Biotech Oncology): Designing and developing early- and late-phase oncology clinical studies, including protocols, clinical development documents, study analyses, and regulatory reports with an accent on molecular targeted and immunological therapies, clinical trial execution, and scientific communication. Focus on coordinating investigators and study teams, interpreting safety and clinical data, preparing publications and health authority submissions, and addressing complex drug development challenges.

Location: Remote within U.S. geographic markets; requires 10–25% travel.

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

Company

hirify.global is a biotechnology company developing investigational oncology therapies and supporting clinical research programs.

What you will do

  • Design, prepare, and initiate early- and late-phase oncology clinical studies, including protocols, synopses, informed consent forms, case report forms, and study documentation.
  • Collaborate with clinical operations, medical monitors, investigators, thought leaders, and project teams throughout clinical development.
  • Research and select investigators, coordinate study activities, and maintain relationships with clinical study sites.
  • Review and interpret clinical and safety data for regulatory submissions, study reports, and close-out documentation.
  • Author and review abstracts, publications, presentations, training materials, and scientific meeting content.
  • Provide scientific presentations and clinical education on investigational oncology agents and monitor emerging clinical and competitive trends.

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 with clinical oncology studies involving molecular targeted or immunological therapies.
  • Detailed knowledge of clinical trial implementation, drug development, GCP, and good medical practice.
  • Experience designing, executing, and reporting oncology trials involving small- and large-molecule drug candidates.
  • Strong analytical, business communication, organization, public speaking, and presentation skills.

Culture & Benefits

  • Remote work arrangement with collaboration across clinical and project teams.
  • Comprehensive employee benefits, including a 401(k) plan with company contributions.
  • Medical, dental, vision, life, disability, and flexible spending account coverage.
  • Discretionary annual bonus program and opportunities to purchase company stock and receive long-term incentives.
  • 15 accrued 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.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →