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5 дней назад

Clinical Research Coordinator - Breast Oncology Clinical Trials

48 100 - 54 400$
Формат работы
hybrid
Тип работы
fulltime
Грейд
junior
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 Coordinator - Breast Oncology Clinical Trials (Clinical Research/Oncology): Coordinating breast oncology clinical trials across start-up, active conduct, data management, monitoring, and close-out with an accent on protocol compliance, patient information, regulatory submissions, and trial sample handling. Focus on managing clinical data and source documents, preparing for audits, coordinating cross-functional study activities, and supporting participant interactions.

Location: Boston, Massachusetts, United States; onsite with occasional remote work

Salary: $48,100–$54,400 per year

Company

hirify.global conducts cancer research, provides patient care, and advances treatment through education and collaboration with Harvard Medical School-affiliated hospitals.

What you will do

  • Coordinate breast oncology clinical trials throughout the study life cycle, from protocol start-up and site activation through close-out.
  • Collect, manage, enter, and report patient clinical data, source documents, case report forms, adverse events, and study activity in clinical trial management systems.
  • Prepare and maintain participant and regulatory binders, IRB submissions, study records, and audit and monitoring materials.
  • Collect, prepare, and ship protocol-required tissue and other samples in accordance with IATA/DOT regulations.
  • Coordinate with scheduling, materials management, laboratories, pharmacy, research nursing, sponsors, regulatory authorities, and other departments.
  • Screen participants, support informed consent for non-treatment trials, register study participants in ONCORE, and conduct protocol-directed patient interactions.

Requirements

  • Bachelor’s degree or one year of Dana-Farber Associate Clinical Research Coordinator experience.
  • Strong organization, communication, interpersonal, prioritization, and follow-through skills.
  • Ability to work with attention to detail, discretion, and hospital confidentiality requirements.
  • Computer skills, including Microsoft Office.
  • Experience in a medical or scientific research setting is preferred; 0–1 years of experience is preferred.
  • Some travel may be required.

Culture & Benefits

  • Inclusive, diverse, and equitable environment focused on compassionate patient care.
  • Work supporting cancer research, public health programs, and treatment breakthroughs.
  • Collaboration with Harvard Medical School-affiliated hospitals and other research partners.
  • Regular onsite work with occasional remote work.

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