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2 дня назад

Director, Clinical Sciences, Oncology (Clinical Development)

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): Supporting Phase 1–3 oncology clinical programs through study strategy, design, execution, data review, and regulatory documentation with an accent on clinical data quality, protocol development, and cross-functional governance. Focus on leading clinical study activities, ensuring data integrity for regulatory submissions, and coordinating global site execution and inspection readiness.

Location: Cambridge, Massachusetts, or Princeton, New Jersey; expected to be in-office 70% of the time with flexibility to work from home up to 30%. Travel up to 15% is required. Only U.S. persons are eligible due to U.S. export control requirements.

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

Company

hirify.global develops mRNA-based medicines and operates a biotechnology platform focused on transforming medicine creation and delivery.

What you will do

  • Support oncology clinical development strategy, trial design, and execution across Phase 1–3 programs.
  • Author and review protocols, informed consent documents, DSURs, Investigator Brochures, INDs, and marketing application materials.
  • Oversee clinical studies, including data review, analysis, interpretation, and timely delivery of study milestones.
  • Coordinate clinical data verification across case report forms, data listings, medical coding, and patient profiles.
  • Collaborate with Clinical Operations and Clinical Safety & Pharmacovigilance on site management, safety decisions, enrollment, and inspection readiness.
  • Develop investigator meeting and advisory board content while training junior Clinical Science personnel.

Requirements

  • PhD, PharmD, master’s, or advanced nursing degree with significant scientific and clinical oncology expertise.
  • At least 10 years of clinical development experience in a pharmaceutical or biotechnology company.
  • Significant experience in clinical study design, protocol development, data integrity, analysis, and presentation.
  • Comprehensive knowledge of drug development and the ability to contribute to early- and late-stage programs.
  • Strong written, oral, presentation, interpersonal, and cross-functional collaboration skills in a matrix environment.
  • Must qualify as a U.S. person under U.S. export control laws; visa sponsorship for non-U.S. persons is unavailable.

Culture & Benefits

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

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