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1 день назад

Senior Clinical Development Medical Director (Oncology)

283 000 - 402 000$
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
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Описание вакансии

Текст:
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TL;DR
Senior Clinical Development Medical Director (Oncology): Leading and executing early- and late-stage oncology clinical trials, including protocol design, medical monitoring, safety analysis, and regulatory reporting with an accent on clinical strategy and scientific interpretation. Focus on designing controlled oncology studies, analyzing trial data and adverse events, and maintaining alignment across cross-functional development teams.

Location: Remote within the United States, with San Francisco listed as a location

Salary: $283,000–$402,000 annually, with compensation varying by U.S. geographic market.

Company

hirify.global is a biotechnology company developing oncology products and conducting clinical research.

What you will do

  • Lead and execute early- and late-stage clinical trials for oncology products.
  • Design, prepare, and initiate clinical study protocols and supporting documentation in compliance with federal regulations, GCP, and good medical practice.
  • Act as medical monitor for company-sponsored trials and monitor protocol adherence through study completion.
  • Analyze and interpret clinical trial and safety data in collaboration with internal safety teams.
  • Prepare reports for regulatory agencies and scientific publications.
  • Collaborate with clinical teams, key opinion leaders, investigators, and cross-functional stakeholders on oncology development strategies.

Requirements

  • MD required; oncology or hematology/oncology board certification or eligibility is desirable but not essential.
  • Minimum eight years of post-residency experience required.
  • Experience in drug development within biotechnology, pharmaceuticals, academia, or a combination of these environments.
  • Hands-on experience designing, executing, and reporting controlled oncology clinical trials.
  • Experience with molecularly targeted or immunological therapies and knowledge of biochemistry, immunology, molecular biology, or genetics.
  • Ability to work effectively in a cross-functional or matrix environment, communicate with senior stakeholders, and develop relationships with key opinion leaders.

Culture & Benefits

  • Collaborative office environment supporting close teamwork, idea sharing, and problem-solving.
  • Equipment provided, including dual monitors and ergonomic chairs.
  • Employee benefits include 401(k) contributions, medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
  • Eligibility for an annual discretionary bonus, company stock purchase opportunities, and long-term incentives.
  • Fifteen accrued vacation days in the first year, seventeen paid holidays including a company-wide winter shutdown, and up to ten sick days annually.

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