Назад
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6 дней назад

Senior Manager, Clinical Scientist, Hematology

Формат работы
onsite/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
Senior Manager, Clinical Scientist, Hematology (Clinical Research): Leading the design, execution, and interpretation of clinical studies for rare hematologic and immunologic diseases with an accent on clinical strategy, medical and safety data review, and cross-functional development programs. Focus on authoring protocols and clinical study reports, applying GCP and regulatory standards, and guiding risk mitigation across the trial lifecycle.

Location: Tarrytown, New York, or Warren, New Jersey, United States. Primarily onsite with hybrid flexibility.

Company

hirify.global is a biotechnology company developing and commercializing medicines for serious and rare diseases.

What you will do

  • Lead the design, execution, and interpretation of clinical studies across early- and late-stage development programs.
  • Partner with Medical Directors, Clinical Study Teams, and Global Clinical SubTeams to define study strategy and scientific direction.
  • Author and review protocols, amendments, clinical study reports, and other key clinical documents.
  • Drive medical and safety data review throughout the trial lifecycle to support patient safety.
  • Represent Clinical Sciences in scientific advisory boards, steering committees, and safety monitoring meetings.
  • Mentor junior team members and support process improvements within Clinical Sciences.

Requirements

  • Bachelor’s degree in life sciences or healthcare; an advanced degree such as PhD, MD, PharmD, or MSc is preferred.
  • At least 8 years of pharmaceutical clinical drug development experience.
  • Knowledge of GCP, clinical study design, and clinical research methodology.
  • Strong scientific and analytical skills for complex clinical development challenges.
  • Ability to ensure compliance with FDA, EMEA, ICH, and GCP standards.
  • Experience in rare hematologic conditions and/or immunologic diseases is preferred.

Culture & Benefits

  • Science-driven work focused on therapies for rare and underserved patient populations.
  • Inclusive workplace and equal employment opportunity practices.
  • Benefits may include incentive plans, equity awards, retirement benefits, health and wellness programs, insurance, paid time off, and family support.
  • Reasonable accommodation is available during recruitment for applicants with known disabilities or chronic illnesses.

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