Назад
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8 часов назад

Director, Clinical Sciences, Oncology

183 800 - 330 300$
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
Director, Clinical Sciences, Oncology (Clinical Development): Directing and evaluating Phase 1–3 oncology clinical studies while ensuring comprehensive clinical data quality for governance decisions and regulatory submissions with an accent on study design, protocol development, data integrity, and regulatory documentation. Focus on leading global study execution, interpreting clinical data, managing safety and site-performance decisions, and training junior Clinical Science personnel.

Location: Cambridge, Massachusetts, or Princeton, New Jersey, United States; 70% in-office and up to 30% work from home

Salary: $183,800–$330,300 per year, plus potential bonus, incentive compensation, or equity.

Company

hirify.global develops mRNA technology and medicines through a biotechnology platform focused on transforming drug creation and delivery.

What you will do

  • Support oncology therapeutic programs and contribute to Phase 1–3 clinical development strategy, trial design, and study execution.
  • Author and review clinical protocols, informed consent documents, DSURs, Investigator Brochures, INDs, and marketing application materials.
  • Oversee clinical studies, including clinical data review, analysis, interpretation, case report form review, medical coding, and patient-profile assessment.
  • Collaborate with Clinical Safety & Pharmacovigilance and study sites on treatment discontinuation and safety decisions.
  • Support global study start-up, site activation, enrollment, inspection readiness, audits, and regulatory inspections.
  • Develop content for Investigator Meetings, investigator engagement, and Advisory Board meetings while training junior Clinical Science personnel.

Requirements

  • PhD, PharmD, master’s degree, or advanced nursing degree with significant scientific and clinical oncology knowledge.
  • At least 10 years of clinical development experience in a pharmaceutical or biotechnology company.
  • Significant experience in clinical study design, protocol development, data integrity, data analysis, and data presentation.
  • Strong written, oral, presentation, interpersonal, and cross-functional collaboration skills in a matrix environment.
  • Ability to work across early- and late-stage programs with Drug Discovery, Translational Medicine, Regulatory Affairs, Biostatistics, Medical Affairs, and Commercial teams.
  • Must qualify as a U.S. person under U.S. export control laws; non-U.S. persons cannot be sponsored for an export control license. Travel up to 15% is required.

Culture & Benefits

  • 70/30 in-office work model emphasizing collaboration, innovation, teamwork, and mentorship.
  • Competitive healthcare and voluntary benefit programs.
  • Fitness, mindfulness, and mental health support.
  • Family planning benefits, including fertility, adoption, and surrogacy support.
  • Paid vacation, volunteer days, sabbatical, global recharge days, and discretionary year-end shutdown.
  • Savings and investment programs, plus location-specific perks.

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