Назад
Company hidden
5 дней назад

VP, Head of Preclinical Development

294 483 - 386 511$
Формат работы
hybrid
Тип работы
fulltime
Грейд
head
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
VP, Head of Preclinical Development (Cell and Gene Therapy): Leading global preclinical development for cell therapy and gene therapy programs from candidate nomination through IND-enabling studies with an accent on pharmacology, toxicology, and regulatory strategy. Focus on integrating PK, PD, safety, and biodistribution data, overseeing GLP studies, building scientific teams, and preparing nonclinical sections of IND applications.

Location: Hybrid role based in Somerset, New Jersey, United States. Applicants must be authorized to work in the United States; employment eligibility is verified through E-Verify.

Base salary: $294,483–$386,511 per year. Performance-based bonus and/or equity may also be available.

Company

hirify.global is a global biotechnology company developing cell therapies for hematological malignancies, solid tumors, and autoimmune diseases, including CAR-T, TCR-T, NK-cell, and other emerging platforms.

What you will do

  • Define and execute the global preclinical development strategy from candidate nomination through IND-enabling studies.
  • Set scientific standards for in vitro pharmacology, in vivo pharmacology, toxicology, experimental design, and data interpretation.
  • Lead preclinical development for lentiviral vector-based in vivo CAR-T, ex vivo cell therapies, and gene-modified immune cell platforms.
  • Integrate PK, PD, safety, and biodistribution data to support clinical strategy, dose selection, regulatory submissions, and portfolio decisions.
  • Own the preclinical components of IND applications, including pharmacology and toxicology summaries, study tabulations, and written nonclinical summaries.
  • Build, lead, and mentor an integrated team of scientists, toxicologists, and embedded CRO personnel.

Requirements

  • PhD in pharmacology, toxicology, immunology, cell biology, or a closely related discipline.
  • At least 15 years of progressive preclinical drug development experience, including 5 years in a senior leadership role accountable for IND-enabling programs.
  • Deep expertise in at least two of three core functions: in vitro pharmacology, in vivo pharmacology, and toxicology.
  • Experience designing, overseeing, and interpreting GLP toxicology studies, including repeat-dose NHP or rodent studies, safety pharmacology, and genotoxicity.
  • Experience in cell therapy, gene therapy, or advanced therapy development, with a record of successful IND submissions and accountability for nonclinical sections.
  • Experience managing CRO relationships and building high-performing scientific teams in a biotech environment.

Culture & Benefits

  • Permanent full-time employees receive medical, dental, and vision insurance.
  • 401(k) retirement plan with a company match that vests fully on day one.
  • Eight weeks of paid parental leave after three months of employment.
  • Paid vacation, personal time, sick time, floating holidays, and eleven company holidays.
  • Additional benefits include flexible spending and health savings accounts, disability coverage, commuter benefits, family planning resources, and well-being programs.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →