Clinical Research Nurse II - Phase II-III Trials

University of Minnesota

Minneapolis (MN)

On-site

USD 78,000 - 95,000

Full time

14 days+
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Job summary

The University of Minnesota is seeking a Research Nurse II to lead nursing expertise in late-phase clinical trials (II-III) with potential for Phase I exposure, ensuring patient safety and data integrity under GCP.

The role involves site initiation, protocol interpretation, patient recruitment and education, coordination with staff and IDS, and accurate documentation in EMR, with a focus on quality and compliance. Requires RN license and nursing degree.

Qualifications

  • BA/BS in Nursing plus at least two years of experience or a combination of education and experience equivalent to 6 years.
  • Current license to practice as a Registered Nurse in the State of Minnesota.
  • Experience with Microsoft Office.
  • Ability to work independently, make decisions, problem solve and prioritize the simultaneous management of multiple clinical studies.
  • Possess excellent communication skills; verbal and written.
  • Flexibility with work schedule to accommodate subject visits.
  • Proof of non-active tuberculosis and immunization per Fairview Research Administration requirements.

Responsibilities

  • Utilizes nursing education to contribute to study start-up activities, including site initiation visits and protocol review.
  • Provides nursing expertise to interpret and operationalize the research protocol.
  • Collaborates with PI and study team to recruit, screen and enroll study participants.
  • Executes study-required procedures in collaboration with clinical staff.
  • Educates patients and clinical staff about treatment plans, side effects, and monitoring guidelines.
  • Maintains accurate source documentation in the EMR (consent/re-consent, adverse events, etc.).
  • Coordinates tracking for patient visits and data collection.
  • Identifies and reports adverse events, stopping rules and protocol deviations per timelines.
  • Troubleshoots problems in protocol procedures.
  • Participates in sponsor visits and monitoring visits.
  • Coordinates with IDS, BioNet and other departments to deliver drug and collect specimens.
  • Communicates effectively within the study team.

Skills

Communication skills
Problem solving
Independent work
Time management

Education

BA/BS in Nursing

Tools

Microsoft Office

Job description

The University of Minnesota is seeking a Research Nurse II to lead nursing expertise in late-phase clinical trials (II-III) with potential for Phase I exposure, ensuring patient safety and data integrity under GCP.

The role involves site initiation, protocol interpretation, patient recruitment and education, coordination with staff and IDS, and accurate documentation in EMR, with a focus on quality and compliance. Requires RN license and nursing degree.

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