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Research Nurse Coordinator

2 months ago

Washington, Washington, D.C., United States Bon Secours Mercy Health Full time
Job Summary

Bon Secours Mercy Health is seeking a skilled Clinical Research Nurse to join our team. As a Clinical Research Nurse, you will play a critical role in the coordination and implementation of clinical trials, ensuring the highest level of quality and patient care.

Key Responsibilities
  • Participate in marketing efforts with local physician groups to identify potential protocol candidates.
  • Maintain a master list of all candidates, active, follow-up, and survival protocol patients.
  • Develop and maintain systems for data retrieval, submission, summary, and analysis for in-house protocols.
  • Maintain, organize, and archive protocol charts.
  • Interface with other disciplines to facilitate accurate and timely data submission.
  • Contact patients and physician offices to verify patient protocol compliance related to follow-up tests/exams as required by the protocol.
  • Ensure, in collaboration with physicians, that eligible patients are enrolled and that informed consent, pre-treatment evaluation, and preparation of candidate patients is completed and properly documented.
  • Maintain accurate and up-to-date knowledge of various studies and participation requirements.
  • Utilize clinical experience and physical skills to assess the physiological status of patients and identify their educational, psychological, and spiritual needs.
  • Instruct patients and their significant others regarding treatments, surgical procedures, nursing plans, interventions, and tests to alleviate apprehension and elicit cooperation.
  • Clarify and carry out physician's orders in a timely manner.
  • Initiate and follow through with problem-solving strategies that lead to resolution of patient care issues.
Requirements
  • Master's degree in nursing or related field preferred.
  • Five years of clinical or related experience.
  • Excellent written and interpersonal communication skills.
  • Proficient in the use of Windows-based MS Office (Word and Excel).
  • Familiar with the use of standard office equipment.
  • Comprehensive understanding of medical terminology.
  • Experience in the use of clinical trial protocols preferred.
  • Demonstrates ability to coordinate and prioritize diverse tasks.
  • Ability to interpret data, adapt, and apply guidelines of research principles.
Working Conditions

The individual performing this job may anticipate coming into contact with human blood and other potentially infectious materials. Individuals in this position are required to exercise universal precautions, use personal protective equipment and devices, and learn the policies regarding infection control.

Travel will be required between various offices.