RN Study Coordinator Day AD/DIP – Radiology Research

Mayo Career Site USRochester, MN
61d

About The Position

The RN Study Coordinator (RN) is accountable for the coordination and delivery of nursing care, including direct patient care, research participant/family education in clinical and research settings. The RN is responsible for managing and/or participating in all phases of the research process. The RN supports professional nursing practice across practice settings and across the continuum of care to meet the needs of the research participant and family, as appropriate. The American Nurses Association (ANA) Standards of Care and Professional Performance provide a basis for practice. The RN understands and advocates for human subject rights. Work is primarily self-directed with guidance from the staff physicians and/or principal investigators. The RN participates in designing, organizing, and monitoring protocols; assists with grant applications, abstracts, posters, and manuscripts; and plans for and participates in staff education in areas where protocols will be carried out. The RN assesses research participants, investigates abnormal patterns of adverse events and laboratory results, and reports appropriately. The RN interacts with other departments to develop systems/procedures for coordinating phases of study protocols that comply with regulatory laws and institutional guidelines for study data collection, storage, retrieval, and participant medical tests and procedures.

Responsibilities

  • Coordination and delivery of nursing care
  • Direct patient care
  • Research participant/family education
  • Managing and/or participating in all phases of the research process
  • Designing, organizing, and monitoring protocols
  • Assisting with grant applications, abstracts, posters, and manuscripts
  • Planning for and participating in staff education
  • Assessing research participants
  • Investigating abnormal patterns of adverse events and laboratory results
  • Reporting appropriately
  • Interacting with other departments to develop systems/procedures for coordinating phases of study protocols
  • Complying with regulatory laws and institutional guidelines for study data collection, storage, retrieval, and participant medical tests and procedures
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