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3 часа назад

Clinical Research Project Manager (Thoracic Oncology)

76 910 - 85 295$
Формат работы
remote (только USA)
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
Clinical Research Project Manager (Thoracic Oncology): Managing multi-center, PI-initiated thoracic oncology clinical trials with an accent on trial startup, regulatory compliance, site coordination, and study documentation. Focus on maintaining Trial Master Files, developing protocols and consent forms, designing case report forms, and coordinating active and close-out phases.

Location: 100% remote, with work permitted only from Maine, Vermont, New Hampshire, Massachusetts, Connecticut, or Rhode Island. The position is never performed on campus.

Salary: $76,910.00–$85,295.00 per year

Company

hirify.global conducts cancer research, patient care, medical education, and public health programs in partnership with Harvard Medical School-affiliated hospitals.

What you will do

  • Manage the day-to-day operations, budgets, resources, timelines, and milestones of assigned thoracic oncology clinical trials.
  • Coordinate startup, active, and close-out phases for PI-initiated and multi-center studies.
  • Develop and maintain Trial Master Files and ensure compliance with Good Clinical Practice standards and institutional requirements.
  • Support protocol and informed consent form development, regulatory submissions, safety-event tracking, and communication with regulatory authorities.
  • Design case report forms, maintain study databases, and prepare protocol-related reports and data summaries.
  • Coordinate research meetings, conference calls, site staff training, mailings, and collaboration with internal and external stakeholders.

Requirements

  • Bachelor’s degree required, preferably in a field related to clinical research.
  • At least three years of clinical research or project management experience, ideally involving multi-center oncology trials.
  • Understanding of clinical trial processes, regulatory requirements, Good Clinical Practice, ethical considerations, and patient confidentiality.
  • Familiarity with clinical trial management tools such as EPIC and OnCore, along with data management and documentation standards.
  • Strong organizational, time-management, communication, problem-solving, and collaboration skills.
  • Must work remotely from one of the permitted New England states: ME, VT, NH, MA, CT, or RI.

Culture & Benefits

  • Fully remote work with no campus attendance required.
  • Work in an innovative, caring, inclusive, and equitable environment.
  • Support a mission focused on reducing the burden of cancer and improving patient care.
  • Collaborate with research partners, including Harvard Medical School-affiliated hospitals.

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