3 часа назад
Associate Director - Director, In Vivo Pharmacology
200 000 - 260 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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