Назад
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3 часа назад

Associate Director, Clinical Science

175 000 - 226 000$
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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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR
Associate Director, Clinical Science (Clinical Development/Translational Science): Planning and overseeing early- and late-stage clinical development programs for genetically engineered porcine organs with an accent on scientifically rigorous protocols, cross-functional execution, and regulatory submissions. Focus on integrating preclinical, translational, and clinical data, reviewing complex clinical datasets, ensuring protocol compliance, and advancing clinical programs through INDs, BLAs, and related regulatory interactions.

Location: Cambridge, MA, United States; hybrid workplace

Base pay range: $175,000–$226,000 per year

Company

hirify.global is a clinical-stage biotechnology company developing human-compatible engineered organs to address the global organ shortage.

What you will do

  • Plan, implement, and oversee early- and late-stage clinical development projects.
  • Develop clinical development plans integrating preclinical, translational, and clinical data.
  • Design rigorous, operationally feasible, and cost-effective clinical protocols.
  • Represent Clinical Science on cross-functional teams and partner with the Medical Monitor on study conduct, progress, and protocol compliance.
  • Lead clinical data review, evaluation, and analysis with Data Management, Biostatistics, and Statistical Programming.
  • Contribute to INDs, BLAs, briefing documents, safety and annual reports, and responses to regulatory agencies.

Requirements

  • PharmD or PhD with 7+ years of clinical science experience in a biotech, pharmaceutical company, or CRO environment.
  • Experience in clinical development and/or translational science.
  • Strong understanding of clinical trial design, data collection standards, and GCP guidelines.
  • Strong analytical skills for analyzing and compiling complex clinical data.
  • Experience working with vendors and clinical sites.
  • Excellent communication, collaboration, leadership, Excel, and PowerPoint skills.

Culture & Benefits

  • Collaborative, science-driven biotech environment.
  • Cross-functional work with internal teams and external partners.
  • Focus on continuous improvement in clinical development processes and study execution.

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