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5 дней назад

Clinical Research Coordinator II (Pediatric Oncology)

56 000 - 63 700$
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 II (Pediatric Oncology) (Clinical Trials/Research): Coordinating pediatric oncology clinical trials from start-up and IRB submissions through data management, monitoring, patient contact, and close-out with an accent on protocol compliance, clinical data collection, and biological sample handling. Focus on preparing regulatory documentation, resolving data queries, coordinating cross-functional trial activities, and supporting audits and study monitoring.

Location: Boston, Massachusetts; hybrid work with 2–3 days onsite per week

Salary: $56,000–$63,700 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

  • Coordinate clinical trials throughout the full study lifecycle, from protocol start-up and site activation through close-out.
  • Support Scientific Review Committee and IRB submissions, regulatory reporting, study documentation, and trial binder maintenance.
  • Collect, manage, report, and validate clinical trial data, including source documents, case report forms, adverse events, and data queries.
  • Collect, prepare, and ship protocol-related samples, including tissue samples, in accordance with trial requirements and IATA/DOT regulations.
  • Collaborate with scheduling, materials management, laboratory, pharmacy, nursing, sponsors, regulatory authorities, and other research departments.
  • Interact with adult and pediatric study participants, support informed consent and eligibility screening when required, and prepare for audits and monitoring visits.

Requirements

  • Bachelor’s degree or two years of experience as a Dana-Farber Clinical Research Coordinator.
  • 1–3 years of relevant experience, preferably in medical or scientific research or a technology-oriented business environment.
  • Excellent organizational, communication, interpersonal, time-management, and prioritization skills.
  • Strong attention to detail, discretion, and adherence to hospital confidentiality guidelines.
  • Computer skills, including Microsoft Office.
  • Ability to work in Boston with 2–3 days onsite per week and interact with patients of all ages and backgrounds.

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.
  • Work with clinical research professionals and partner institutions affiliated with Harvard Medical School.
  • Responsibilities include orienting and assisting with training new staff.

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