обновлено 5 дней назад
VP, Head of Preclinical Development (Biotech)
294 483 - 386 511$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
VP, Head of Preclinical Development (Biotech): Leading global preclinical development for cell and gene therapy programs across in vitro pharmacology, in vivo pharmacology, and toxicology with an accent on IND-enabling studies, regulatory submissions, and scientific leadership. Focus on integrating PK, PD, safety, and biodistribution data, designing GLP toxicology programs, and building high-performing preclinical teams.
Location: Hybrid role based in Somerset, New Jersey, United States
Salary: $294,483–$386,511 USD base pay annually, plus performance-based bonus and/or equity for eligible employees
Company
is a global biotechnology company developing cell therapies for hematological malignancies, solid tumors, and autoimmune diseases, including CAR-T, TCR-T, NK cell-based, and other advanced therapy platforms.
What you will do
- Define and execute preclinical development strategies across pipeline programs 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 into compound narratives that support clinical strategy, dose selection, and regulatory submissions.
- 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 pharmacology scientists and toxicologists, including internal staff 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 senior leadership with direct accountability 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 assessments.
- Experience in cell therapy, gene therapy, or advanced therapy development, with a record of successful IND submissions and accountability for nonclinical sections.
- Must be authorized to work in the United States; employment eligibility is verified through Form I-9 and E-Verify.
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, sick, floating holiday, and company holiday time.
- Additional benefits include flexible spending and health savings accounts, disability coverage, family planning resources, well-being initiatives, and commuter benefits.
- Benefits are available exclusively to permanent full-time employees; contractors are not eligible.
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