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2 дня назад

Clinical Research Coordinator - GI Oncology

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 - GI Oncology (Clinical Trials): Coordinating phase I–IV GI oncology clinical trials and managing patient clinical data, regulatory documentation, protocol samples, and study records with an accent on Good Clinical Practice, IRB compliance, and cross-functional trial operations. Focus on screening patients, obtaining informed consent, resolving data queries, preparing audits, and coordinating studies throughout the trial life cycle.

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

Salary: $48,100–$54,400 per year

Company

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

What you will do

  • Coordinate phase I–IV clinical trials across gastrointestinal cancers under the direction of the Principal Investigator.
  • Manage clinical data, source documents, case report forms, adverse event reporting, data queries, and study records.
  • Support trial start-up, Scientific Review Committee and IRB submissions, site activation, monitoring, audits, and study close-out.
  • Collect, prepare, and ship protocol-required blood and tissue samples in accordance with IATA/DOT regulations.
  • Screen patients for eligibility, obtain informed consent, register participants, and communicate with study participants as required.
  • Coordinate with sponsors, regulatory authorities, research nursing, pharmacy, laboratories, scheduling, and materials management.

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 primarily onsite in Boston, with occasional remote work.
  • May involve contact with adult and pediatric patients and some travel.

Culture & Benefits

  • Inclusive, diverse, and equitable environment focused on compassionate patient care.
  • Work within a clinical research program advancing cancer treatment and public health.
  • Collaboration with Harvard Medical School-affiliated hospitals and multiple clinical research departments.
  • Equal opportunity employment with consideration for qualified applicants regardless of protected characteristics.

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