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3 часа назад

Associate Director - Director, In Vivo Pharmacology

200 000 - 260 000$
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

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TL;DR
Associate Director - Director, In Vivo Pharmacology (AI-designed gene editing therapeutics): Leading rodent and non-human primate studies for customized base editor programs with an accent on editing activity, delivery, biodistribution, durability, tolerability, and translational biomarkers. Focus on CRO study execution, cross-functional data interpretation, candidate selection, dose strategy, and IND-enabling development planning.

Location: Emeryville, California, United States; on-site

Salary: $200,000–$260,000 USD annually

Company

hirify.global is an AI biology company building foundation models for biological molecules and developing AI-designed gene editing medicines.

What you will do

  • Lead in vivo pharmacology strategy for customized base editor programs across rodent and non-human primate studies, from proof of concept through candidate nomination and IND-enabling planning.
  • Design and oversee studies assessing editing efficiency, delivery, biodistribution, exposure, dose response, durability, pharmacodynamic biomarkers, tolerability, and translational relevance.
  • Represent in vivo pharmacology on cross-functional teams and translate complex datasets into recommendations for candidate selection, dose rationale, and development strategy.
  • Manage external CRO and vivarium execution, including protocols, vendor oversight, monitoring, sample logistics, data quality control, troubleshooting, and report review.
  • Integrate NGS, ddPCR/qPCR, RNA and protein, histology, clinical chemistry, cytokine, immunology, and other study readouts with partner teams and CROs.
  • Build scalable pharmacology processes and contribute to regulatory-facing packages while mentoring researchers.

Requirements

  • PhD or equivalent in pharmacology, physiology, molecular biology, genetics, bioengineering, or a related field, plus 6–8 years of relevant industry experience.
  • Experience designing, managing, and interpreting rodent and non-human primate pharmacology studies and supporting IND-enabling studies.
  • Experience with genetic medicines, including genome editing, base editing, gene therapy, RNA medicines, oligonucleotides, LNP delivery, or viral vectors.
  • Strong understanding of PK/PD, dose response, biodistribution, target engagement, pharmacodynamic biomarkers, translational endpoints, and preclinical development strategy.
  • Experience leading CRO studies and operating as a senior cross-functional scientific leader.
  • Applicants must already have ongoing United States work authorization that does not require employer sponsorship.

Culture & Benefits

  • Competitive compensation with equity participation.
  • 401(k) with a strong employer match.
  • Health, dental, and vision insurance.
  • Generous paid time off and a commitment to work-life balance.
  • Professional development in the AI and biology field.

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