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4 дня назад

Senior Medical Director, Hematology Clinical Development (Biotech)

182 000 - 346 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior/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
Senior Medical Director, Hematology Clinical Development (Biotech): Leading the planning, execution, and interpretation of hematology clinical development programs with an accent on clinical strategy, study integrity, regulatory compliance, and cross-functional scientific leadership. Focus on designing protocols and development plans, interpreting safety and efficacy data, guiding regulatory submissions, and coordinating global clinical research activities.

Location: South San Francisco, California, United States

Salary: $182,000–$346,000 USD per year in base pay.

Company

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

What you will do

  • Lead the planning, design, execution, and interpretation of hematology clinical development programs.
  • Oversee clinical study integrity, enrollment, timelines, safety reporting, and evaluation of efficacy and safety data.
  • Develop and review protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions, and related scientific documents.
  • Build clinical development plans and contribute to translational strategies, due diligence, and business development activities.
  • Provide clinical expertise across cross-functional teams and engage external opinion leaders in the relevant disease area.
  • Ensure compliance with regulatory requirements, Good Clinical Practices, pharmacovigilance standards, and quality 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 manage a clinical research program of moderate complexity with minimal supervision.
  • Ability to collaborate effectively on global cross-functional teams and support scientific and business strategy.
  • Excellent oral and written English communication skills required.

Nice to have

  • Completion of a residency program.
  • Completion of a subspecialty fellowship.

Culture & Benefits

  • Cross-functional collaboration across clinical, scientific, regulatory, medical affairs, commercial, and discovery functions.
  • Opportunities to participate in conferences, medical literature review, and professional training.
  • Paid vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) and eligibility for long-term incentive programs.

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