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4 дня назад

Chief Medical Officer (CMO)

450 000 - 480 000$
Формат работы
onsite/hybrid
Тип работы
fulltime
Грейд
c_level
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Chief Medical Officer (AI-powered clinical development): Architecting and leading end-to-end clinical development strategy for AI-enabled therapeutics, including Phase 1 and Phase 2 trials, with an accent on patient selection, dosing, biomarkers, and regulatory strategy. Focus on designing adaptive, basket, and Bayesian trials, integrating AI/ML into clinical execution, and building a high-performance global clinical development organization.

Location: South San Francisco, California, United States. The role is either onsite approximately 3 days per week or hybrid with onsite presence for 1–2 weeks per month.

Salary: $450,000–$480,000 per year, plus annual performance bonus and equity incentive plan eligibility.

Company

hirify.global is a physical AI drug discovery and development company using machine learning, multimodal biological data, and human genetics to develop therapeutics and clinical strategies.

What you will do

  • Architect and lead the end-to-end clinical development strategy across therapeutic areas and modalities.
  • Build, scale, and mentor a clinical development organization spanning medical, translational, biomarker, safety, regulatory, and clinical operations functions.
  • Design and oversee clinical trial protocols, Investigator Brochures, clinical development plans, and ongoing trial execution.
  • Develop AI-powered adaptive, basket, and Bayesian trial methodologies to optimize patient stratification, dosing, and operational efficiency.
  • Lead Medical Affairs, Pharmacovigilance, Regulatory Affairs, patient safety, and interactions with agencies including the FDA and EMA.
  • Provide clinical and strategic guidance across target validation, indication selection, late-stage development, partnerships, investor communications, and post-marketing activities.

Requirements

  • MD or equivalent degree with board certification in a therapeutically relevant area.
  • 20+ years of progressive clinical development experience in the pharmaceutical or biotechnology industry.
  • Proven record of successful IND and NDA/BLA submissions and significant strategic involvement in an approved New Chemical Entity.
  • Direct experience designing and delivering Phase 1 and Phase 2 trials, establishing human proof of concept, and applying biomarkers and adaptive trial designs.
  • Deep knowledge of global regulatory requirements and successful collaboration with regulatory agencies.
  • Experience applying AI/ML and data science methods in clinical trials, biomarker discovery, regulatory submissions, or clinical operations.
  • Experience building high-performance teams and working across large biopharma organizations and agile startups.

Nice to have

  • Experience in metabolic disease or neuroscience.
  • Board certification or therapeutic expertise in cardiometabolic disease or neuroscience.
  • Experience communicating with investors and collaborating with academic institutions and key opinion leaders.

Culture & Benefits

  • Annual performance bonus plan and equity incentive plan.
  • 401(k) plan with employer matching and medical, dental, vision, and mental health coverage.
  • Flexible vacation policy and paid parental leave.
  • Quarterly budget for books and online courses, plus a home-office setup stipend.
  • Monthly cell phone and internet stipend, onsite meals and baristas, and commuter bus access across the Bay Area.

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