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12 дней назад

Assistant Clinical Research Manager - Breast Oncology Clinical Trials

70 000 - 85 300$
Формат работы
hybrid
Тип работы
fulltime
Грейд
middle
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
Assistant Clinical Research Manager - Breast Oncology Clinical Trials (Clinical Research): Supporting the management of breast oncology clinical trials across startup, active treatment, follow-up, and closeout phases with an accent on regulatory compliance, data management, and staff supervision. Focus on maintaining audit-ready trial portfolios, tracking protocol milestones, monitoring patient enrollment and data quality, and coordinating clinical research staff training.

Location: Hybrid, with 2–3 days onsite per week in Boston, Massachusetts; remote days may only be worked from Maine, Vermont, New Hampshire, Massachusetts, Connecticut, or Rhode Island.

Salary: $70,000–$85,300 per year

Company

hirify.global conducts cancer research, provides patient care, educates physician-researchers, and collaborates with Harvard Medical School-affiliated hospitals.

What you will do

  • Assist the Clinical Research Manager with oversight of the breast oncology clinical trial portfolio.
  • Support study startup, active treatment, follow-up, and closeout activities, including protocol milestone tracking.
  • Monitor patient enrollment, registration, protocol treatment, follow-up care, and related trial processes.
  • Maintain regulatory documentation, reporting systems, and an audit-ready research environment.
  • Support data management, compliance monitoring, progress reporting, and corrective actions.
  • Assist with coordinator recruitment, staff supervision, onboarding, training, and competency assessments.

Requirements

  • Bachelor’s degree.
  • 3+ years of related experience preferred.
  • Understanding of clinical trial startup, active, and closeout phases.
  • Knowledge of clinical research, cancer treatment modalities, local policies, and federal and state regulations.
  • Experience with protocol development, data compilation and analysis, and clinical trial tracking systems.
  • Ability to work independently, think critically, exercise professional judgment, and communicate effectively.

Culture & Benefits

  • Work in an innovative, caring, inclusive, and equitable healthcare and research environment.
  • Contribute to cancer research and patient care across diverse populations.
  • Hybrid work arrangement with scheduled onsite presence in Boston.
  • Potential contact with patients of all ages and backgrounds.

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