Clinical Trials Coordinator & Research Specialist

UNC Health

Raleigh (NC)

Presencial

USD 37 000 - 53 000

Tempo integral

Há 2 dias
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Resumo da oferta

UNC Health in North Carolina is seeking a Clinical Research Coordinator to join the Cancer Center Research Raleigh team. This full-time role supports studies by coordinating resources, educating patients and families, and ensuring adherence to protocols and regulatory requirements.

Responsibilities include reviewing protocols, obtaining informed consent, and assisting with audits while applying evidence-based practices to improve trial quality. Onsite work, 40 hours weekly, salary range listed.

Qualificações

  • Bachelor's degree in a clinical/health-related field required.
  • Two years of clinical research experience or equivalent.
  • Ability to read and interpret safety rules, procedures and manuals.

Responsabilidades

  • Reviews protocols to determine availability of resources, subjects and equipment needs.
  • Educates patients and families about clinical trials and goals; communicates with physicians.
  • Obtains written informed consent with HIPAA authorization prior to enrollment.
  • Conducts study per protocol; follows data collection guidelines and regulatory requirements.
  • Participates in sponsor audits and regulatory inspections of records.
  • Recognizes and utilizes evidence-based clinical practices.

Conhecimentos

Statistical reporting
Data analysis/interpretation
Data verification
Data coding - general
Reading comprehension

Formação académica

Bachelor's degree in a clinical/health-related field

Descrição da oferta de emprego

UNC Health in North Carolina is seeking a Clinical Research Coordinator to join the Cancer Center Research Raleigh team. This full-time role supports studies by coordinating resources, educating patients and families, and ensuring adherence to protocols and regulatory requirements.

Responsibilities include reviewing protocols, obtaining informed consent, and assisting with audits while applying evidence-based practices to improve trial quality. Onsite work, 40 hours weekly, salary range listed.

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