Назад
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6 дней 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 Research/Oncology): Supporting Phase 1–3 oncology clinical development programs by directing study execution, evaluating clinical data, and ensuring data quality for governance decisions and regulatory submissions with an accent on clinical study design, protocol development, and regulatory documentation. Focus on coordinating global trial operations, interpreting clinical data, managing site safety decisions, and building inspection-ready studies.

Location: Cambridge, MA or Princeton, NJ, United States; 70% in-office with 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-based medicines and vaccines across infectious diseases, immuno-oncology, rare diseases, and cardiovascular diseases.

What you will do

  • Support Oncology Therapeutic programs and the Clinical Development Lead across Phase 1–3 clinical studies.
  • Contribute to clinical program strategy, trial design, protocol development, and study execution.
  • Author and review protocols, informed consent documents, DSURs, Investigator Brochures, INDs, and marketing application materials.
  • Lead or support clinical study oversight, clinical data review and analysis, data interpretation, and verification of case report forms, listings, coding, and patient profiles.
  • Coordinate with Clinical Operations, Clinical Safety, Pharmacovigilance, and study sites to support treatment decisions, enrollment, inspections, and audit readiness.
  • Develop content for Investigator Meetings, investigator engagement, and Advisory Boards while training junior Clinical Science personnel.

Requirements

  • PhD, PharmD, Master's degree, or advanced nursing degree with substantial clinical oncology and drug development 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.
  • Experience working in matrix environments and collaborating with Drug Discovery, Translational Medicine, Regulatory Affairs, Biostatistics, Medical Affairs, and Commercial functions.
  • Ability to travel up to 15% and work from a U.S. office location under the 70/30 in-office model; only U.S. persons eligible due to export-control requirements.

Culture & Benefits

  • In-person collaboration model focused on innovation, teamwork, and direct mentorship.
  • Healthcare and voluntary benefit programs.
  • Fitness, mindfulness, mental health, family planning, fertility, adoption, and surrogacy support.
  • Paid time off including vacation, volunteer days, sabbatical, global recharge days, and year-end shutdown.
  • Savings and investment programs plus location-specific perks.

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