RN - Clinical Research

Carle BroMenn Medical Center

Normal, ILFull-time

Behavioral Health Market Context

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Job Description

nning, implementation, and management of clinical research studies.
• Screen, recruit, and obtain informed consent from study participants.
• Provide direct patient care, monitor patient responses, and ensure safety in accordance with study protocols.
• Administer investigational drugs, treatments, and procedures as per study guidelines.
• Collect, document, and report clinical data accurately in case report forms and electronic databases.
• Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and institutional review board (IRB) guidelines.
• Educate patients and their families about study procedures, risks, and benefits.
• Collaborate with multidisciplinary teams, including physicians, research coordinators, and sponsors.
• Monitor for adverse events, report findings, and assist in resolving protocol deviations.
• Maintain study records, regulatory documentation, and research logs.
• Participate in site audits, monitoring visits, and quality assurance initiatives.

Qualifications

    Benefits

      Responsibilities

      • The RN Clinical Research Nurse plays a crucial role in supporting clinical trials by ensuring compliance with protocols, providing patient care, and coordinating research activities
      • This position involves working closely with principal investigators, study coordinators, and regulatory bodies to facilitate the safe and ethical conduct of research studies
      • Assist in the planning, implementation, and management of clinical research studies
      • Screen, recruit, and obtain informed consent from study participants
      • Provide direct patient care, monitor patient responses, and ensure safety in accordance with study protocols
      • Administer investigational drugs, treatments, and procedures as per study guidelines
      • Collect, document, and report clinical data accurately in case report forms and electronic databases
      • Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and institutional review board (IRB) guidelines
      • Educate patients and their families about study procedures, risks, and benefits
      • Collaborate with multidisciplinary teams, including physicians, research coordinators, and sponsors
      • Monitor for adverse events, report findings, and assist in resolving protocol deviations
      • Maintain study records, regulatory documentation, and research logs
      • Participate in site audits, monitoring visits, and quality assurance initiatives


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