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3 дня назад

Clinical Research Coordinator II - WoMB

47 924 - 59 894$
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 II - WoMB (Clinical Research): Supporting the Principal Investigator in planning and implementing clinical research studies with an accent on participant recruitment, eligibility screening, regulatory documentation, and clinical data collection. Focus on coordinating study procedures, maintaining protocol compliance, resolving data queries, and monitoring adverse events.

Location: Tufts Medical Center; typical clinical and administrative office setting

Salary: $47,924.24–$59,894.75 annually based on full-time equivalent

Company

hirify.global provides clinical and research services, including support for human-subjects clinical studies.

What you will do

  • Assist the Principal Investigator with planning and implementing assigned clinical research studies.
  • Recruit, screen, interview, and follow up with study participants in clinic, by telephone, and in other required settings.
  • Review eligibility criteria, explain studies, obtain informed consent, and coordinate required tests and procedures.
  • Abstract source documents, complete case report forms, perform data entry, conduct quality checks, and resolve data queries.
  • Support IRB submissions, regulatory binders, adverse-event reporting, sponsor site visits, and protocol compliance.
  • Perform basic laboratory activities and trained procedures such as EKGs and walk tests while maintaining study supplies and confidentiality.

Requirements

  • Bachelor’s degree, or a high school diploma or equivalent with four years of related experience.
  • At least two years of experience in research-related activities.
  • Basic Life Support certification may be required for specific role requirements.
  • Strong organizational, data collection, record-keeping, communication, interpersonal, and computer skills.
  • Ability to prioritize tasks, maintain meticulous attention to detail, and follow HIPAA, FDA Good Clinical Practice, and human-subject protection requirements.

Nice to have

  • Five years of research-related experience.
  • Previous clinical trials 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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