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Clinical Development Medical Director (Hematology)

239 900 - 399 800$
Формат работы
hybrid
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
Clinical Development Medical Director (Hematology) (Late-Phase Clinical Trials): Leading the design, conduct, and analysis of late-phase hematology clinical trials with an accent on medical oversight, clinical data interpretation, and cross-functional development strategy. Focus on monitoring patient safety, guiding investigators and study teams, and resolving complex clinical, ethical, and regulatory challenges.

Location: Hybrid role based in New York City, United States, requiring residence within commuting distance and on-site work an average of 2.5 days per week. Candidates must have permanent authorization to work in the United States. U.S. visa sponsorship is not available.

Salary: $239,900–$399,800 annual base salary, plus a 25% bonus target and eligibility for a share-based long-term incentive program.

Company

hirify.global is a global pharmaceutical company developing medicines and vaccines across multiple therapeutic areas.

What you will do

  • Provide clinical development leadership across two to three hematology study teams.
  • Oversee medical monitoring, eligibility assessment, clinical data review, and safety monitoring.
  • Lead peer-to-peer discussions with investigators and address clinical issues with study teams, ethics committees, steering committees, and regulatory authorities.
  • Develop and maintain clinical trial and regulatory documents with clinical scientists and cross-functional partners.
  • Interpret clinical data, identify key findings, and communicate implications to internal and external stakeholders.
  • Advise current and future clinical development plans using current medical literature, guidelines, and clinical expertise.

Requirements

  • Clinical development experience.
  • Medical degree such as MD, DO, MBBS, or MBChB from a recognized medical school or university.
  • At least four years of experience after obtaining a medical degree.
  • Medical license allowing independent prescription of medicines for at least two years after internship, house officer, or foundation training.
  • Permanent U.S. work authorization is required; TN, O-1, H-1B, and other U.S. visa sponsorship is unavailable.

Nice to have

  • Late-stage clinical development experience.
  • Hematology experience.
  • Board certification or eligibility in oncology or an equivalent qualification.

Culture & Benefits

  • Cross-functional collaboration with regulatory affairs, pharmacovigilance, biostatistics, medical affairs, oncology teams, and external stakeholders.
  • Opportunities to influence peers, coach colleagues, and guide work toward meaningful clinical and business outcomes.
  • Comprehensive benefits including a 401(k) with company matching and an additional retirement savings contribution.
  • Paid vacation, holidays, personal days, caregiver and parental leave, and medical leave.
  • Medical, prescription drug, dental, and vision coverage.
  • Travel to conferences and team meetings approximately four times per year; relocation assistance may be available based on eligibility and business needs.

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