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45 минут назад

Scientific Associate Director - Project Toxicologist (Biotech)

194 274 - 262 841$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
director
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
Scientific Associate Director - Project Toxicologist (Biotech): Developing and implementing fit-for-purpose nonclinical safety strategies for innovative therapeutics across discovery, development, and post-marketing with an accent on translational risk assessment, regulatory strategy, and multidisciplinary leadership. Focus on designing complex safety studies, interpreting experimental data, integrating AI-enabled approaches and New Approach Methodologies, and supporting first-in-human applications and marketing authorizations.

Location: United States — Remote

Annual salary: USD 194,274.30–262,841.70

Company

hirify.global is a biotechnology company developing and delivering innovative medicines for serious illnesses across oncology, inflammation, general medicine, rare disease, and other therapeutic areas.

What you will do

  • Serve as the Translational Safety & Risk Sciences representative on core project teams and lead the related scientific sub-team.
  • Develop, implement, oversee, and interpret nonclinical safety assessment programs for drug development candidates.
  • Design innovative study strategies addressing complex scientific questions, including AI-enabled approaches and New Approach Methodologies.
  • Evaluate experimental data and author nonclinical strategy, governance, and regulatory submission sections.
  • Communicate scientific recommendations across project teams, leadership, governance bodies, regulatory agencies, and external partners.
  • Support business development evaluations and mentor scientists in nonclinical studies and development programs.

Requirements

  • Doctorate degree in PhD, PharmD, or MD with at least 4 years of toxicology experience; or master’s degree with 7 years; or bachelor’s degree with 9 years.
  • Experience with drug development and nonclinical safety assessment across multiple therapeutic areas and modalities.
  • Ability to lead cross-functional teams, influence scientific decisions, and operate in a matrixed environment.
  • Experience interpreting data and supporting regulatory submissions, including first-in-human applications and marketing authorizations.
  • Strong written and verbal scientific communication skills.

Nice to have

  • At least 8 years of experience as a Project Toxicologist or Nonclinical Safety Project Team Representative across all development stages.
  • Experience with siRNA therapeutics, antibody-drug conjugates, antibody-peptide conjugates, or targeted protein degraders.
  • Subject matter expertise in a defined toxicology area, such as drug-induced liver injury.
  • American Board of Toxicology certification, external publications or presentations, and business development due diligence experience.

Culture & Benefits

  • Collaborative, innovative, and science-based work environment.
  • Health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Annual bonus program and stock-based long-term incentives.
  • Paid time off and career development opportunities.
  • Flexible work models, including remote and hybrid arrangements where possible.

Hiring process

  • Applications are accepted until a sufficient number of applications are received or a candidate is selected.
  • Sponsorship is not guaranteed.

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