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5 дней назад

Senior Scientist II (Pharmacology) (Oncology)

132 500 - 188 000$
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

Текст:
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TL;DR
Senior Scientist II (Pharmacology) (Oncology): Leading in vivo pharmacology research for oncology drug discovery and development projects with an accent on PK/PD/efficacy studies, rodent tumor models, and preclinical characterization. Focus on designing and interpreting complex animal experiments, establishing PK/PD/efficacy relationships, preparing IND filing documentation, and coordinating CRO and project-team activities.

Location: Alameda HQ, Alameda, California, United States; office-based role

Salary: $132,500–$188,000 annually, with the range varying by U.S. geographic market.

Company

hirify.global develops therapeutic candidates and supports oncology drug discovery and development programs.

What you will do

  • Lead, design, execute, and interpret in vivo pharmacology studies covering PK, PD, and efficacy in rodent tumor models.
  • Establish PK/PD/efficacy relationships and characterize toxicity profiles using preclinical animal models.
  • Represent Pharmacology or serve as Project Team Co-Lead on Discovery project teams.
  • Design and test drug-target hypotheses using scientific literature and internal datasets.
  • Coordinate studies with contract research organizations and prepare pharmacology reports supporting IND filings.
  • Support animal facility and laboratory operations, collaborate with IACUC, and ensure animal welfare compliance.

Requirements

  • PhD in Pharmacology, Cancer Biology, Molecular and Cellular Biology, or a closely related field, plus at least two years of industrial experience after postdoctoral training, or equivalent experience.
  • Deep knowledge of in vivo pharmacology for oncology drug discovery and extensive experience with xenograft, syngeneic, genetically engineered mouse, orthotopic, PDX, and humanized tumor models.
  • Experience writing regulatory and IND filing documents for preclinical pharmacology.
  • Expertise in experimental design, data analysis, cell culture with aseptic technique, animal handling, dosing, blood and tissue collection, necropsy, tumor measurement, and rodent survival surgery.
  • Required understanding of IACUC and AAALAC regulations and guidelines.
  • Managerial experience leading a small group of 3–5 people is required.

Nice to have

  • Strong publication record and broad scientific expertise.
  • Experience coaching junior scientists and working across multidisciplinary project teams.

Culture & Benefits

  • Collaborative office environment focused on sharing ideas and solutions.
  • Medical, dental, vision, life, disability, and flexible spending benefits.
  • 401(k) plan with company contributions and eligibility for an annual discretionary bonus.
  • Company stock purchase opportunities and long-term incentives.
  • Fifteen vacation days in the first year, seventeen paid holidays, and up to ten sick days annually.
  • Work may include weekends and holidays to support in vivo studies; equipment includes dual monitors and ergonomic chairs.

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