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2 дня назад

Clinical Research Coordinator - Breast Oncology Cohorts Program (Breast 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 - Breast Oncology Cohorts Program (Breast Oncology) (Clinical Research): Coordinating breast oncology clinical trials from protocol start-up through close-out, including patient data collection, regulatory submissions, sample handling, and study documentation with an accent on Good Clinical Practice, IRB compliance, and clinical trial data management. Focus on screening and consenting participants, resolving data queries, preparing for audits and monitoring visits, and coordinating protocol-specific samples in accordance with IATA/DOT regulations.

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 collaboration with Harvard Medical School-affiliated hospitals.

What you will do

  • Coordinate clinical trials throughout the full lifecycle, from protocol receipt and start-up through site activation and close-out.
  • Collect, manage, and report patient clinical data, source documents, case report forms, adverse events, and data queries.
  • Prepare and maintain participant and regulatory binders, study records, clinical trial management system entries, and IRB submissions.
  • Screen patients for eligibility, obtain informed consent for non-treatment trials, register participants in ONCORE, and support protocol-related patient interactions.
  • Collect, prepare, and ship clinical and tissue samples in accordance with protocol requirements and IATA/DOT regulations.
  • Coordinate with research, laboratory, pharmacy, nursing, scheduling, materials management, sponsors, and regulatory authorities; prepare for audits and monitoring visits.

Requirements

  • Bachelor’s degree or one year of Dana-Farber Associate Clinical Research Coordinator experience.
  • Excellent organizational, communication, interpersonal, time-management, and prioritization skills.
  • Strong attention to detail, follow-through, discretion, and adherence to hospital confidentiality guidelines.
  • Computer proficiency, including Microsoft Office.
  • Ability to work onsite in Boston with occasional remote work and interact with adult and pediatric study participants.

Culture & Benefits

  • Work in an innovative, caring, inclusive, diverse, and equitable clinical research environment.
  • Contribute to cancer research, patient care, public health programs, and treatment advances.
  • Collaborate with Harvard Medical School-affiliated hospitals and multidisciplinary research departments.
  • Some travel may be required.

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