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5 часов назад

Sr. Clinical Trial Manager, Therapeutics and Oncology

130 800 - 209 400$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
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
Sr. Clinical Trial Manager, Therapeutics and Oncology (clinical trial management): Overseeing complex therapeutic and oncology clinical trials across multiple regions with an accent on vendor management, study timelines, clinical data review, and ICH/GCP compliance. Focus on leading cross-functional trial teams, managing CRO oversight and feasibility, and ensuring quality, budget, and delivery milestones.

Location: Princeton, New Jersey, United States; hybrid 70/30 work model with 70% in-office collaboration. Only U.S. persons are eligible due to U.S. export control requirements.

Salary: $130,800–$209,400 per year, with potential eligibility for an annual discretionary bonus, incentive compensation, or equity award.

Company

hirify.global develops mRNA-based medicines and technologies for transforming how medicines are created and delivered.

What you will do

  • Manage and oversee assigned clinical trials across all phases, ensuring quality, compliance, timelines, and deliverables.
  • Lead clinical trial teams and represent Clinical Operations on cross-functional development teams.
  • Manage CRO and vendor oversight, trial feasibility, site capability assessments, monitoring reports, and study-level documentation.
  • Review clinical data, quality metrics, deviations, study systems, and trial samples to support data review and operational readiness.
  • Manage study timelines, budgets, invoices, forecasting, dashboards, and status reporting for senior management.
  • Support clinical documents, operational workstreams, continuous improvement initiatives, and collaborative stakeholder relationships.

Requirements

  • 5–7 years of experience in clinical research and the pharmaceutical or biotechnology industry, including at least 2 years of independent trial management.
  • Bachelor’s degree required; advanced degree preferred.
  • Robust oncology and rare disease experience required; immuno-oncology and high-complexity experience such as CAR-T are desirable.
  • Strong understanding of drug development, project management, FDA requirements, and ICH/GCP guidelines.
  • Excellent verbal and written communication, organizational skills, and attention to detail.
  • Must qualify as a U.S. person and be able to access export-controlled information; visa sponsorship is not available.

Culture & Benefits

  • 70/30 in-office work model supporting collaboration, teamwork, and mentorship.
  • Healthcare and voluntary benefits programs.
  • Fitness, mindfulness, mental health, and broader well-being resources.
  • Family planning benefits, including 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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