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7 дней назад

Distinguished Scientist, Nonclinical Safety Leader

164 000 - 282 900$
Формат работы
hybrid
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
Distinguished Scientist, Nonclinical Safety Leader (Toxicology/Pharmacology): Leading nonclinical safety and toxicology strategy across drug discovery and development projects with an accent on risk assessment, safety pharmacology, regulatory documentation, and cross-functional leadership. Focus on analyzing toxicology data, preparing human safety assessments, resolving complex safety issues, and supporting clinical trials and global registrations.

Location: Hybrid role based in Spring House, Pennsylvania, or Cambridge, Massachusetts, United States

Base pay: $164,000–$282,900 per year

Company

Johnson & Johnson Innovative Medicine develops medicines and healthcare solutions across multiple therapeutic areas and innovative modalities.

What you will do

  • Lead project teams of nonclinical safety and pharmacokinetic scientists and ensure effective information transfer.
  • Represent nonclinical safety on global, multidisciplinary project teams, providing toxicology expertise and strategic matrix leadership.
  • Create target risk assessments, develop risk mitigation plans, and analyze toxicology and safety pharmacology studies for human safety implications.
  • Generate hypotheses and investigative strategies for issue-resolution teams and contribute to medical safety, signal detection, and risk mitigation activities.
  • Prepare global regulatory nonclinical documents and health authority responses supporting clinical trials and compound registrations.
  • Collaborate with discovery, CMC, regulatory, licensing and acquisition, academic, and industry stakeholders while mentoring scientists and leading strategic initiatives.

Requirements

  • Master’s degree in Toxicology, Pharmacology, or a related discipline; a PhD, DVM, MD, or equivalent doctoral degree is preferred.
  • At least 15 years of relevant pharmaceutical or biotech industry experience with a Master’s degree, or at least 10 years with a doctoral degree.
  • Proven experience representing toxicology or nonclinical safety on multidisciplinary project teams.
  • Strong understanding of the drug discovery and development process.
  • Excellent written and oral communication skills and the ability to collaborate across organizational levels.
  • Experience with due diligence, GLP study direction or monitoring, emerging therapeutic modalities, and toxicology board certification is preferred.

Culture & Benefits

  • Inclusive work environment focused on diversity, dignity, and individual contribution.
  • Participation in a consolidated retirement plan, pension, savings plan, and 401(k), subject to plan terms.
  • Eligibility for the long-term incentive program.
  • Paid vacation, sick time, holidays, personal and family time, parental leave, bereavement leave, caregiver leave, volunteer leave, and military spouse time-off, subject to applicable policies.

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