Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Выше рынка
$232к-348к/год
$150к$170кмедиана$210к
По похожим ролям (49) ~ $170к/год
90
Крутая вакансия
развернуть
Чётко очерченная научная лидерская роль в известной биотех-компании даёт возможность влиять на стратегию и наставлять коллег; главный барьер - очень высокий требуемый опыт.
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Требуют большой стажВлияние на стратегиюИзвестная биотех-компанияПоддержка развитияВыше рынка
Оценка от Hirify AI
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Toxicology Senior Research Fellow (Biotech): Leading preclinical safety assessment for novel molecules and therapies across research programs, with an accent on small molecule toxicology, in vivo and in vitro study design, and cross-functional project strategy. Focus on designing early safety strategies, interpreting study results, overseeing external CRO studies, and guiding compounds toward candidate nomination and early development.
Location: San Diego, CA; hybrid position requiring 3 days per week onsite, with an onsite option of 5 days per week.
Base salary: $232,000–$348,000 per year, plus eligibility for annual bonus and annual equity awards.
Company
Vertex is a global biotechnology company focused on scientific innovation and developing therapies for patients.
What you will do
Lead Preclinical Safety Assessment (PSA) activities on research project teams, cross-site teams, steering committees, and disease-area or site strategies.
Develop early safety assessment strategies for multiple programs from target selection through development and candidate nomination.
Design appropriate in vivo and in vitro safety studies and collaborate with cross-functional and cross-site partners on portfolio-specific strategies.
Coordinate required studies and profiling assays, interpret findings, and communicate results to project teams, site management, and PSA leadership.
Provide scientific oversight of external studies at CROs and partner organizations and collaborate with regulatory toxicologists during the transition from research into development.
Prepare reports and presentations, monitor scientific and industry developments, mentor toxicologists and research scientists, and contribute to site scientific leadership.
Requirements
Subject matter expertise in small molecule toxicology and in the design and interpretation of in vivo studies in common preclinical species.
In-depth knowledge of animal husbandry and animal welfare issues.
Excellent data processing and statistical skills.
Excellent written, verbal communication, and influencing skills.
Proficiency with Microsoft Office Suite or equivalent office productivity tools.
Bachelor’s, Master’s, or Doctoral degree in life sciences or chemistry.
Typically, a Bachelor’s degree with 20 years of experience, a Master’s degree with 15 years of experience, or a PhD with 11 years of experience.
Nice to have
DABT certification.
Culture & Benefits
Hybrid work with the option to work remotely up to two days per week, or work onsite five days per week with ad hoc flexibility.
Medical, dental, and vision benefits, paid time off, and company shutdowns in summer and winter.
Educational assistance programs, including student loan repayment, plus a commuting subsidy.
Continuous learning encouraged across AI, technology, automation, and industry trends.
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