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3 дня назад

Medical Director, Clinical Development (Oncology)

275 000 - 300 000$
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, Clinical Development (Oncology): Advancing registration-enabling clinical studies for palazestrant in ER-positive, HER2-negative breast cancer with an accent on study design, clinical data evaluation, regulatory engagement, and biomarker strategy. Focus on providing medical oversight, ensuring data integrity, collaborating with investigators and cross-functional teams, and translating clinical development strategy into action.

Location: Cambridge, Massachusetts, United States; up to 20% travel may be required.

Base pay: $275,000–$300,000 annually, plus equity, bonus, and benefits.

Company

hirify.global is a clinical-stage biopharmaceutical company developing therapies for breast cancer and other oncology indications, including palazestrant and OP-3136.

What you will do

  • Provide oncology medical leadership for the palazestrant clinical development program.
  • Contribute to registration-enabling study design, protocol development, regulatory submissions, and interactions with investigators and regulatory authorities.
  • Evaluate safety, pharmacology, efficacy, and clinical data to guide program strategy and decision-making.
  • Partner with Clinical Operations, Biostatistics, Safety, CROs, and translational teams to ensure scientific rigor, data integrity, and ethical execution.
  • Support biomarker strategy, publication planning, manuscripts, abstracts, and external scientific communications.
  • Serve as a medical expert for internal and external clinical and scientific questions.

Requirements

  • MD with US Board Certification required.
  • Board certification in Oncology, Hematology/Oncology, or a related specialty.
  • At least 2 years of direct biotech or pharmaceutical clinical development experience; a strong academic background may substitute.
  • Experience designing and managing oncology clinical studies, or significant experience as a principal investigator or academic breast cancer expert.
  • Strong understanding of breast cancer treatment paradigms and the drug development process.
  • Knowledge of GCP, FDA, and EMA/CHMP regulations, with strong communication, problem-solving, collaboration, and organizational skills.

Culture & Benefits

  • Work in a small, agile, mission-driven oncology organization focused on improving patient outcomes.
  • Competitive compensation and benefits package.
  • Equity and bonus opportunities.
  • Open, flexible, and supportive work environment with opportunities for professional growth and leadership development.
  • Equal opportunity workplace that values diverse expertise, backgrounds, and perspectives.

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