Epic-Savvy Clinical Research Coordinator

Hanker Systems, Inc.

Orange (CA)

Híbrido

USD 85 000 - 110 000

Tempo integral

há 42 horas
Torna-te num dos primeiros candidatos

Uma candidatura completa num minuto

Currículo e carta de apresentação personalizados, prontos a enviar.

Ultrapassa os filtros ATS

Vantagens oferecidas por esta oferta de emprego

Hybrid work option

Resumo da oferta

Providence St. Joseph Heritage Medical Group in Orange, CA seeks an experienced Clinical Research Coordinator to oversee multiple studies, with 2+ years in hands-on clinical research, direct patient interaction, and strong Epic experience.

You will coordinate with physicians, sponsors, and IRBs to ensure GCP/ICH compliance. The role involves patient recruitment, informed consent, data entry into EDC systems, sample handling, and accurate study documentation, with a potential hybrid work

Qualificações

  • 2+ years of hands-on clinical research experience with direct patient interaction.
  • Experience coordinating multiple clinical studies and with physicians, sponsors, and IRBs.
  • Must have Epic experience and strong communication/organizational skills.
  • Proficiency with Microsoft Outlook, Teams, Word, and Excel.

Responsabilidades

  • Coordinate day-to-day activities for multiple clinical research studies.
  • Recruit, enroll, and retain study participants and obtain informed consent.
  • Educate patients about trial requirements and ensure compliance with protocols.
  • Schedule patient visits, labs, vitals, and EKGs; maintain accurate study records.

Conhecimentos

Epic experience
Clinical research coordination
Patient interaction
MS Office proficiency (Outlook/Teams/W

Ferramentas

Epic EHR
EDC systems

Descrição da oferta de emprego

Providence St. Joseph Heritage Medical Group in Orange, CA seeks an experienced Clinical Research Coordinator to oversee multiple studies, with 2+ years in hands-on clinical research, direct patient interaction, and strong Epic experience.

You will coordinate with physicians, sponsors, and IRBs to ensure GCP/ICH compliance. The role involves patient recruitment, informed consent, data entry into EDC systems, sample handling, and accurate study documentation, with a potential hybrid work

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