Назад
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10 дней назад

Director, Clinical Development (MD)

261 375 - 338 250$
Формат работы
onsite
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
Director, Clinical Development (MD) (Oncology and CAR T-cell therapy): Leading the execution of multiple clinical trials in hematologic malignancies with an accent on medical monitoring, clinical study design, regulatory interactions, and cross-functional trial delivery. Focus on designing proof-of-concept and first-in-human studies, translating preclinical findings into clinical opportunities, and advancing novel CAR T-cell therapies.

Location: Foster City, California, United States

Salary: $261,375–$338,250 per year for the Bay Area; $237,575–$307,450 per year for other US locations.

Company

hirify.global is a biopharmaceutical company developing cancer immunotherapies, including CAR T-cell and TCR-engineered cell therapies.

What you will do

  • Provide medical monitoring for multiple oncology clinical trials in hematologic malignancies.
  • Lead project teams in designing, implementing, and conducting clinical studies.
  • Write and review protocols, investigator brochures, clinical study reports, and other trial documents.
  • Conduct investigator meetings and site initiation visits, while maintaining relationships with clinical investigators and external sites.
  • Execute drug development strategies, develop contingency plans, provide technical guidance, and manage milestones and budgets.
  • Support regulatory interactions and filings, and collaborate with clinical operations, biomarker specialists, CROs, regulatory affairs, preclinical scientists, translational scientists, business, and commercial teams.

Requirements

  • MD or equivalent qualification.
  • At least 4 years of experience managing oncology trials.
  • Experience in hematology/oncology clinical trials and knowledge of relevant treatment options.
  • Experience designing, implementing, and conducting clinical trials, particularly proof-of-concept and first-in-human studies.
  • Strategic leadership, sound judgment, critical thinking, troubleshooting, and problem-solving skills.
  • Ability to work independently and collaboratively with scientific, technical, clinical, and cross-functional stakeholders.

Nice to have

  • Board certification or specialization in Hematology or Oncology.
  • At least 2 years of relevant drug development experience in industry, academia, or clinical investigation.
  • Experience developing and maintaining relationships with key opinion leaders and clinical investigators.

Culture & Benefits

  • People-focused leadership culture centered on inclusion, employee development, and empowerment.
  • Fast-paced environment with changing priorities and opportunities to take on additional responsibilities.
  • Travel of up to 30% may be required.
  • Eligibility for a discretionary annual bonus and stock-based long-term incentives may apply.
  • Benefits may include medical, dental, vision, and life insurance, as well as paid time off.

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