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4 часа назад

Director/Senior Director, In Vivo Pharmacology (Oncology)

195 000 - 290 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior/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
Director/Senior Director, In Vivo Pharmacology (Oncology): Leading the design, execution, and interpretation of in vivo pharmacology studies for small-molecule oncology programs with an accent on oncology models, PK/PD-driven study design, and translational pharmacology. Focus on integrating tumor efficacy, exposure, biomarkers, tolerability, and mechanism-of-action data to guide candidate nomination and portfolio decisions.

Location: San Francisco, California; on-site

Salary: $195,000–$290,000 annually, plus eligibility for an annual discretionary bonus and equity incentive plan.

Company

hirify.global is a biopharma company developing a disease-agnostic, fully integrated network biology platform using genetics, proteomics, structural biology, and AI to advance drug discovery.

What you will do

  • Lead in vivo pharmacology strategy for small-molecule oncology programs.
  • Design and oversee CDX, PDX, and syngeneic in vivo studies, including model selection, dose and schedule optimization, PK/PD integration, and efficacy assessment.
  • Develop pharmacology plans supporting development candidate nomination, IND readiness, and early clinical translation.
  • Integrate tumor efficacy, exposure, pharmacodynamic biomarkers, tolerability, and mechanism-of-action data to guide compound prioritization and program decisions.
  • Collaborate with biology, medicinal chemistry, DMPK, and external CRO partners.
  • Mentor and potentially manage scientists as the organization grows.

Requirements

  • PhD in pharmacology, cancer biology, molecular biology, physiology, translational medicine, or a related discipline.
  • Typically 10+ years of relevant industry experience in oncology drug discovery or translational pharmacology.
  • Deep expertise in in vivo pharmacology for small-molecule oncology drug discovery.
  • Experience designing and interpreting efficacy, PK/PD, dose-response, dose-scheduling, and mechanism-of-action studies in oncology models.
  • Hands-on experience with rodent oncology models, including CDX, PDX, and syngeneic models.
  • Experience integrating pharmacology with medicinal chemistry, DMPK, biomarker strategy, candidate nomination, and CRO oversight.

Culture & Benefits

  • Collaborative workplace focused on respect, diversity, team science, and shared success.
  • Medical, dental, and vision insurance.
  • Discretionary time off, company holidays, and summer and winter shutdowns.
  • 401(k), commuter or mass transit benefits, and healthcare and dependent care FSAs.
  • Parental leave and a flexible work schedule.

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