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2 дня назад

Clinical Research Coordinator II - Attleboro

56 000 - 62 700$
Формат работы
hybrid
Тип работы
fulltime
Грейд
middle
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 - Attleboro (Clinical Research): Coordinating clinical trials at the Attleboro satellite location with an accent on patient data collection, regulatory documentation, protocol sample handling, and study compliance. Focus on maintaining accurate clinical research records, supporting IRB submissions, screening and consenting eligible participants, and coordinating work across satellite sites.

Location: Attleboro campus, 20 O'Neil Blvd, Attleboro, Massachusetts; onsite work with occasional remote support. Travel to the Longwood campus and other Dana-Farber satellite sites may be required.

Salary: $56,000–$62,700 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 the conduct of clinical trials at the Attleboro satellite location under the direction of principal investigators and disease programs.
  • Collect, manage, and accurately transcribe patient clinical information and study data.
  • Maintain regulatory binders and ensure compliance with state, federal, IRB, ICH/GCP, and institutional requirements.
  • Coordinate protocol-related sample collection and shipment to external entities.
  • Screen patients, obtain informed consent for minimal-risk studies, and register participants when required.
  • Support IRB submissions, train new staff, and provide on-site and remote support across satellite locations.

Requirements

  • Bachelor's degree and 1–3 years of related experience.
  • Understanding of clinical research study coordination, clinical trial phases, CRF completion, and accurate data transcription.
  • Understanding of ICH/GCP, federal regulatory requirements, IRB processes, and DF/HCC standard operating procedures.
  • Excellent organization, communication, interpersonal, time-management, and prioritization skills.
  • Attention to detail, discretion, and adherence to hospital confidentiality guidelines.
  • Computer skills, including Microsoft Office, and the ability to work autonomously with minimal supervision.

Nice to have

  • Experience in a medical, scientific research, or technology-oriented business environment.

Culture & Benefits

  • Inclusive, diverse, and equitable environment focused on compassionate patient care.
  • Work supporting cancer research, treatment advances, public health programs, and underserved populations.
  • Collaboration with Harvard Medical School-affiliated hospitals and other research partners.
  • Combination of onsite work and occasional remote support, with collaboration across satellite locations.

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