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3 дня назад

Clinical Research Coordinator (Clinical Research)

44 778 - 55 978$
Формат работы
onsite
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 (Clinical Research): Supporting the Principal Investigator in planning and implementing clinical research studies with an accent on participant recruitment, eligibility assessment, regulatory documentation, and clinical data collection. Focus on maintaining protocol compliance, coordinating IRB requirements and data queries, and ensuring accurate study records under HIPAA and FDA Good Clinical Practice guidelines.

Location: Tufts Medical Center, United States; typical clinical and administrative office setting.

Salary: $44,778.55–$55,978.47 per year based on full-time equivalent.

Company

hirify.global provides clinical care and conducts basic, translational, and clinical research.

What you will do

  • Assist the Principal Investigator with planning and implementing assigned clinical research studies.
  • Recruit and follow up with study participants, assess eligibility, explain studies, and obtain informed consent.
  • Abstract source records, complete case report forms, enter study data, and coordinate resolution of data queries.
  • Maintain regulatory binders, source documents, study supplies, and other study records.
  • Support IRB submissions, adverse-event reporting, site visits, and protocol-compliance activities.
  • Arrange protocol-required tests and perform appropriate procedures such as EKGs and walk tests.

Requirements

  • Bachelor’s degree, or a high school diploma/equivalent plus four years of related experience.
  • Basic Life Support certification may be required depending on the role requirements.
  • Strong organization, data collection and analysis, record-keeping, computer, prioritization, communication, and interpersonal skills.
  • Meticulous attention to detail and the ability to work with confidential patient and study information.
  • Compliance with HIPAA, FDA Good Clinical Practice guidelines, institutional policies, and human-subject protection regulations.

Nice to have

  • Two years of research-related experience.
  • IATA Hazardous Goods Shipping certification.
  • CITI Human Research Protection certification.

Culture & Benefits

  • Full-time employment with a comprehensive Total Rewards package.
  • Benefits support health, financial security, and career growth.
  • Compensation is determined based on experience, certifications, education, skills, and internal equity.

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