Назад
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9 дней назад

Senior Medical Director, Hematology Clinical Development

211 000 - 400 500$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior/director
Английский
c1
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 Medical Director, Hematology Clinical Development (Clinical Trials/Biotech): Overseeing the design, execution, interpretation, and reporting of hematology clinical development programs with an accent on clinical strategy, patient safety, regulatory compliance, and cross-functional collaboration. Focus on designing protocols and development plans, interpreting safety and efficacy data, guiding regulatory submissions, and ensuring Good Clinical Practice across complex global studies.

Location: North Chicago, Illinois, United States

Salary: $211,000–$400,500 annual base pay

Company

hirify.global develops medicines and solutions for serious health conditions across immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Lead the direction, planning, execution, and interpretation of hematology clinical development programs.
  • Oversee clinical study integrity, enrollment, timelines, safety reporting, and efficacy data interpretation.
  • Design and review protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions, and related scientific documents.
  • Develop cross-functional Clinical Development Plans and contribute to translational strategies and business development activities.
  • Provide medical expertise to internal stakeholders, investigators, opinion leaders, and regulatory discussions.
  • Ensure compliance with Good Clinical Practice, pharmacovigilance standards, regulatory requirements, and internal procedures.

Requirements

  • Medical Doctor, Doctor of Osteopathy, or non-US equivalent degree with a relevant therapeutic specialty.
  • At least 2 years of clinical trial experience in the pharmaceutical industry, academia, or an equivalent setting.
  • Knowledge of clinical trial methodology, regulatory and compliance requirements, clinical strategy, and study protocol design.
  • Ability to lead moderately complex clinical research programs with minimal supervision.
  • Ability to collaborate effectively across global cross-functional teams.
  • Excellent oral and written English communication skills required.

Nice to have

  • Completed residency program.
  • Completed subspecialty fellowship.
  • Experience overseeing Medical Directors, Scientific Directors, or Clinical Scientists.

Culture & Benefits

  • Cross-functional and global scientific collaboration.
  • Paid vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) benefits for eligible employees.
  • Eligibility for long-term incentive programs.

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