Clinical Research Nurse 2

6 days ago

IL United States Rush Full time
Job Summary

We are seeking an experienced Clinical Research Nurse 2 to join our research team at Rush University Medical Center. As a key member of our team, you will provide clinical care within the context of a clinical research study and potentially help develop studies and projects.

Responsibilities
  • Relationships and Caring
    • Provide nursing care to patients participating in clinical research studies, including standard of care procedures, research procedures, study medication administration, and adherence assessments.
    • Create and implement nursing plans of care in connection with study protocols.
    • Utilize clinical assessments to ensure patients receive follow-up care as needed.
    • Communicate research-related information to patients, families, nursing, and medical staff as necessary.
    • Educate physicians and other clinical staff on the study protocol and the plan of care for research participants.
    • Communicate participant health status changes to the Principal Investigator and clinical care staff.
    • Precept and mentor less experienced research nurses or other staff.
  • Evidence-Based Practice
    • Perform subject assessments, administer medication, and provide nursing support to perform diagnostic, therapeutic, and surgical procedures.
    • Schedule visits and ensure study-related orders are completed for the visit, including providing patient education regarding tests and/or procedures.
    • May enter study-related data into appropriate databases.
    • May collect, process, and ship potentially biohazardous specimens.
    • May proactively identify potential issues and/or variances with study protocol regulatory issues.
  • Technical Expertise
    • Maintain current knowledge of disease/disorder-specific conditions and clinical research trends.
    • Attend and participate in study-specific training, conferences, and education.
    • May present at professional conferences related to clinical research.
    • Adhere to attributable, eligible, contemporaneous, original, and accurate (ALCOA) documentation standards.
    • Train members of the study team and departmental clinical staff related to study protocols, policies, and procedures, regulatory guidelines, and regulations.
  • Critical Thinking
    • Assess subject eligibility for inclusion in research protocols, e.g., pre-screening, screening, and enrollment.
    • Obtain informed consent and document according to institutional policy.
    • Ensure the study team is kept up-to-date on the protocol and safety reports received from the study sponsor.
    • Maintain written and verbal communications on a regular schedule with the Principal Investigator and other assigned contacts.
    • Prepare for, participate in routine monitoring visits, audits, etc.
    • May assist in planning new protocols and associated implementation.
  • Leadership
    • Collaborate with the Principal Investigator, sponsor, medical monitor, compliance, staff, Office of Research Affairs, and manager to identify and improve both routine and complex processes as it relates to the regulatory and operational aspects of a research study.
    • Develop, implement, and communicate processes and procedures for data quality assurance and safety monitoring.
    • Accountable to the Principal Investigator for protocol adherence. Help ensure the research team is performing activities within established protocols.
    • May provide training to members of the study team and departmental clinical staff related to study protocols, policies, and procedures.
    • May provide clinical direction to less experienced research and nursing staff.

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