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3 дня назад

Medical Director / Senior Medical Director (Oncology)

285 000 - 390 000$
Формат работы
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
Medical Director / Senior Medical Director (Oncology) (Clinical Development): Advancing oncology molecules through the clinical pipeline and supporting the execution of clinical studies with an accent on clinical strategy, protocol development, regulatory filings, and safety oversight. Focus on leading clinical data reviews, coordinating advisory committees, supporting investigator interactions, and translating clinical research plans into high-quality studies.

Location: Brisbane, California, United States — onsite; up to 25% travel in the US and internationally

Salary: $285,000–$390,000 per year

Company

hirify.global is a clinical-stage biopharmaceutical company developing targeted protein degradation medicines for cancer and inflammatory diseases using an AI-integrated discovery engine.

What you will do

  • Provide scientific guidance to cross-functional clinical development and study teams.
  • Develop and implement global development plans for molecules in the clinical pipeline.
  • Lead the review and authorship of clinical protocols, informed consent documents, study manuals, and investigator meeting materials.
  • Prepare clinical sections of regulatory filings and meeting packages for US and ex-US health authorities.
  • Support clinical data review, data cleaning, analysis, dose-escalation preparation, and safety oversight.
  • Coordinate medical advisory committees, interact with investigators, support site and CRA training, and contribute to manuscripts and presentations.

Requirements

  • Advanced degree in clinical or biological sciences; MD, PhD, or PharmD preferred.
  • 15+ years of relevant drug development experience and at least 5 years of oncology clinical trial experience.
  • Experience with clinical operations, translational medicine, clinical trial design, and oncology development.
  • Strong understanding of ICH GCP and general industry standards.
  • Excellent communication, collaboration, attention to detail, and ability to translate technical concepts for broader study teams.
  • Commitment to patient safety and clinical compliance.

Nice to have

  • Experience with first-in-human and proof-of-concept oncology studies involving small molecules, biologics, or cell therapy.
  • Registrational or Phase 3 study experience.
  • Experience with Spotfire, Medidata Rave, or similar clinical programs.
  • Medical monitoring experience and proficiency with Microsoft Office.

Culture & Benefits

  • Collaborative, strongly team-oriented environment.
  • Solutions- and results-oriented approach.
  • Hands-on, resourceful work style open to diverse points of view.
  • Up to 25% US and international travel.

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