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2 дня назад

Clinical Research Coordinator (Cancer Hematology)

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 (Cancer Hematology) (Clinical Trials): Coordinating cancer hematology clinical trials, collecting and managing patient data, and facilitating protocol assessments with an accent on regulatory compliance, participant screening, and protocol sample handling. Focus on preparing IRB submissions, resolving data queries, organizing audits, and managing studies throughout the trial lifecycle.

Location: Boston, Massachusetts, United States; onsite work with occasional remote work. Some travel to hirify.global satellite sites may be required.

Salary: $48,100–$54,400 per year.

Company

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

What you will do

  • Coordinate cancer hematology clinical trials from protocol receipt and study start-up through activation, conduct, and close-out.
  • Collect, manage, enter, and report patient clinical data, source documents, case report forms, adverse events, and study activity records.
  • Screen patients for eligibility, obtain informed consent for non-treatment trials, register participants in ONCORE, and interact with study participants according to protocol requirements.
  • Collect, prepare, and ship protocol-related tissue and other samples in accordance with trial requirements and IATA/DOT regulations.
  • Prepare IRB and regulatory submissions, maintain trial and regulatory binders, and support compliance with state, federal, and IRB requirements.
  • Coordinate sponsor and regulatory communications, audits, monitoring visits, and collaboration with scheduling, laboratory, pharmacy, nursing, and other departments.

Requirements

  • Bachelor’s degree or one year of Dana-Farber Associate Clinical Research Coordinator experience.
  • Excellent organization, communication, interpersonal, time-management, and prioritization skills.
  • Strong attention to detail, follow-through, discretion, and adherence to hospital confidentiality guidelines.
  • Computer skills, including Microsoft Office.
  • Ability to work with adult and pediatric patients and communicate with study participants as required.

Nice to have

  • 0–1 years of experience in a medical or scientific research setting or comparable technology-oriented business environment.

Culture & Benefits

  • Inclusive, diverse, and equitable environment focused on compassionate patient care.
  • Opportunity to contribute to cancer research and public-health programs for high-risk and underserved populations.
  • Collaboration with clinical, research, academic, and external partner organizations.
  • Full-time employment with a hybrid arrangement that allows occasional remote work.

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