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5 дней назад

Global Clinical Lead (Hematology)

Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
US/Australia
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
Global Clinical Lead (Hematology) (Clinical Development/Biotechnology): Leading global clinical development strategy and providing medical and scientific guidance for hematology programs and 5–8 Global Clinical Program Leaders with an accent on therapeutic-area leadership, regulatory strategy, and clinical program design. Focus on defining development strategies, guiding benefit–risk assessments, supporting regulatory submissions, and coordinating matrixed teams across clinical, non-clinical, commercial, and payer stakeholders.

Location: King of Prussia, Pennsylvania, United States

Company

hirify.global is a global biotherapeutics company developing therapies in hematology, immunology, cardiovascular and metabolic diseases, respiratory conditions, and transplantation.

What you will do

  • Provide strategic and tactical medical and scientific leadership for 5–8 Global Clinical Program Leaders.
  • Represent Clinical Development on the Therapeutic Area Leadership Team for the cardiovascular, respiratory, and related therapeutic area.
  • Define global clinical development strategies and oversee clinical plans, protocols, and program execution.
  • Contribute to business development strategy, due diligence, stage-gate evaluations, and benefit–risk assessments.
  • Ensure high-quality clinical and scientific content for regulatory submissions and interactions with health authorities.
  • Mentor clinical drug developers, build external expert networks, and represent the clinical function at scientific and technical forums.

Requirements

  • MD and board certification, or a non-US equivalent; relevant subspecialty certification is highly preferred.
  • Clinical development experience leading a therapeutic area or complex clinical program.
  • Working knowledge of pharmaceutical and regulatory development processes.
  • At least 8–10 years of experience in industry or academia; academic experience must include work with industry sponsors.
  • Proven leadership, influencing, collaboration, and matrix-management skills.
  • Experience interacting with health authorities and designing programs for health authorities, commercial stakeholders, and payers.

Culture & Benefits

  • Work within a global biotherapeutics organization serving patients in more than 100 countries.
  • Collaborate across clinical, non-clinical, medical affairs, commercial, payer, and therapeutic-area functions.
  • Participate in a culture focused on inclusion, belonging, curiosity, empathy, and scientific innovation.
  • Employee benefits are provided by CSL.

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