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Clinical Lead Early Development and Experimental Therapeutics - Oncology

206 250 - 297 917$
Формат работы
hybrid
Тип работы
fulltime
Грейд
lead
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
Clinical Lead Early Development and Experimental Therapeutics - Oncology (Oncology/Translational Medicine): Designing and leading early clinical development for oncology assets from first-in-human studies through phase 2a, with an accent on proof-of-mechanism, proof-of-concept, biomarker interpretation, and human target validation. Focus on dose escalation, medical safety oversight, cross-functional trial execution, CRO coordination, and translating preclinical findings into clinical studies.

Location: Cambridge, MA or Morristown, NJ; hybrid; US and Puerto Rico residents only

Salary: $206,250–$297,916.66 per year

Company

hirify.global is an R&D-driven biopharmaceutical company developing medicines and vaccines through immunoscience, AI, data, and digital platforms.

What you will do

  • Design and lead early clinical development studies for oncology assets, from first-in-human studies through phase 2a.
  • Develop protocols covering dose escalation, proof-of-mechanism, proof-of-concept, natural history, mechanistic, and signal-seeking studies.
  • Provide clinical expertise for preclinical data interpretation, translational medicine, biomarker research, and human target validation.
  • Make decisions on protocol design, dose selection, study safety, and early Go/No-Go recommendations.
  • Oversee medical monitoring, CROs, clinical operations, study documentation, data review, and clinical study reporting.
  • Coordinate global project teams and collaborate with research, toxicology, pharmacology, regulatory, safety, biostatistics, and biomarker specialists.

Requirements

  • MD or equivalent required.
  • At least 3 years of clinical research experience required.
  • English required.
  • Experience designing or conducting early clinical trials, ideally phase 1/2a oncology studies.
  • Experience with medical safety oversight, translational or biomarker research, and interpretation of preclinical data.
  • Knowledge of GCP practices, cross-functional team leadership, clinical documentation, and work in a matrix organization.

Nice to have

  • MD and PhD or comparable bench science experience.
  • Experience with combination therapies and drugs targeting cytoplasmic signaling pathways.
  • Experience using emerging digital or AI-driven tools and working in a global pharmaceutical environment.
  • Postgraduate residency training, laboratory research, or late-phase clinical trial experience.

Culture & Benefits

  • Work with a future-focused biopharmaceutical research organization addressing unmet needs in oncology.
  • Opportunities for career growth through promotions or international and lateral moves.
  • Healthcare, prevention, wellness, and family benefits, including at least 14 weeks of gender-neutral parental leave.
  • Access to AI, data, and digital platforms supporting drug discovery and development.
  • Collaborative work with investigators, clinical experts, regulatory authorities, CROs, and multidisciplinary internal teams.

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