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3 дня назад

Associate Medical Director or Medical Director (Oncology)

216 000 - 270 000$
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
Associate Medical Director or Medical Director (Oncology) (Clinical Development): Leading execution and medical oversight of a Phase 1 oncology clinical program while supporting pipeline programs preparing for IND submission with an accent on patient safety, regulatory compliance, and clinical data integrity. Focus on reviewing safety and efficacy data, guiding protocol adherence, preparing regulatory and study documents, and coordinating with cross-functional development teams and external clinical partners.

Location: Remote - US

Salary: Associate Medical Director: $216,000–$270,000 per year; Medical Director: $248,000–$310,000 per year.

Company

hirify.global Therapeutics is a clinical-stage life-science and technology company developing novel medicines through an AI-driven discovery and development platform.

What you will do

  • Provide medical monitoring and scientific oversight throughout assigned clinical trials, including a Phase 1 clinical program.
  • Review adverse events, serious adverse events, protocol deviations, patient eligibility, and clinical data to support participant safety and study integrity.
  • Collaborate with clinical operations, regulatory sciences, data management, biostatistics, clinical pharmacology, and nonclinical teams to execute studies.
  • Contribute to protocols, amendments, Investigator Brochures, informed consent forms, clinical study reports, and regulatory submissions.
  • Support regulatory agency interactions, advisory boards, scientific presentations, abstracts, and manuscripts.
  • Build strategic partnerships with key opinion leaders, centers of excellence, and patient advocacy organizations.

Requirements

  • MD or PharmD with clinical oncology experience and biotech or pharmaceutical oncology drug-development experience preferred; alternatively, a PhD with at least three years of biotech or pharmaceutical oncology drug-development experience.
  • Experience serving as a medical monitor, including patient eligibility review, site interaction, protocol adherence oversight, deviation review, clinical data review and cleaning, and coding.
  • Experience executing clinical studies and interacting with regulatory agencies.
  • Excellent written and verbal communication, organizational, time-management, and problem-solving skills.
  • Ability to work effectively with cross-functional internal and external partners and manage multiple tasks with strong attention to detail.
  • Must be based in the United States for this remote role.

Culture & Benefits

  • Inclusive environment focused on diversity of backgrounds, cultures, and life experiences.
  • Company-paid healthcare and flexible spending accounts.
  • 401(k) matching and voluntary life insurance.
  • Uncapped vacation.
  • Access to a state-of-the-art San Diego facility with an onsite gym and dining.

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