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7 дней назад

Senior Scientist / Scientist, In Vivo Pharmacology (Biotech)

130 000 - 180 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Senior Scientist / Scientist, In Vivo Pharmacology (Biotech): Designing and executing in vivo pharmacology studies for epigenetic reprogramming therapeutics with an accent on PK/PD, efficacy, dose-response, and translational animal models. Focus on interpreting in vivo data, refining aging and disease models, overseeing CRO studies, and supporting preclinical candidate selection and regulatory-enabling work.

Location: South San Francisco, United States

Salary: $130,000–$180,000 per year

Company

hirify.global is a biotechnology company developing medicines for age-related diseases by reprogramming the epigenome and restoring regenerative potential in aged and diseased cells.

What you will do

  • Design, execute, and interpret in vivo pharmacology studies covering PK/PD, efficacy, and dose-response across disease models and therapeutic programs.
  • Evaluate epigenetic reprogramming payloads in relevant animal models with epigenetic editing, predictive modeling, and therapeutic area teams.
  • Develop and refine animal models of aging and age-related disease for translational studies.
  • Oversee study design, protocols, and CRO or vendor relationships.
  • Analyze pharmacology data, biomarkers, and functional endpoints to guide preclinical decisions.
  • Contribute to regulatory-enabling study design and documentation as programs advance toward clinical development.

Requirements

  • Ph.D. in pharmacology, physiology, biology, or a related field, or equivalent industry experience.
  • 5+ years of experience for Scientist or 8+ years for Senior Scientist.
  • Demonstrated experience designing and executing in vivo pharmacology studies in rodent models, including PK, PD, efficacy, and dose-range finding.
  • Experience with study design, dosing regimens, route-of-administration selection, and in vivo data interpretation.
  • Experience leading project workflows and mentoring junior laboratory staff.
  • Experience contributing to a preclinical or clinical drug development program.

Nice to have

  • Experience with liver biology, hepatic disease models, or hepatocyte-directed delivery.
  • Experience with nucleic acid or viral vector delivery in vivo.
  • Experience with GLP-enabling or IND-enabling study design.
  • Experience with single-cell genomics or pooled screening approaches applied to in vivo readouts.

Culture & Benefits

  • Health, dental, and vision insurance.
  • 401(k) with company match.
  • Paid parental leave.
  • 20 days of paid time off per year plus holidays.
  • Meals and snacks provided on site.

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