Clinical Trials Nursing Specialist

3 weeks ago

Vancouver, British Columbia, Canada The University of British Columbia Full time

Position Overview

The Clinical Research Nurse collaborates with Research Coordinators, Assistants, and fellow Nurses to facilitate clinical trials aimed at advancing knowledge in Multiple Sclerosis (MS) and Neuromyelitis Optica (NMO). This role operates under the guidance of the MS Research Manager and is accountable to the Director of the MS Clinical Trials Group.

Key Responsibilities

  • Engage with Study Investigators to review research protocols and study designs.
  • Screen, register, and conduct ongoing assessments of research participants in alignment with study protocols.
  • Collect participant data and complete necessary documentation, including case report forms and charts.
  • Support departmental personnel to ensure compliance with study requirements.
  • May be involved in the collection of biological samples and the review of test results.

Organizational Context

This role requires independent work within established ethical and competent research practices. The Clinical Research Nurse will report to the Research Manager and the Director of MS Clinical Trials, ensuring adherence to guidelines set forth by the MS Clinical Trials group.

Work Duties

  • Implement and instruct study staff on protocols.
  • Draft and review Informed Consent Forms for participants.
  • Educate staff on safety measures for subjects.
  • Coordinate recruitment, screening, and enrollment of suitable participants.
  • Attend educational sessions to inform MS patients about ongoing clinical trials.
  • Document informed consent in accordance with Good Clinical Practice (GCP).
  • Act as a liaison with the Research Manager, Principal Investigator, sponsors, and Contract Research Organizations (CROs).
  • Manage study supplies and maintain inventory.
  • Ensure compliance with regulatory bodies and maintain quality documentation.
  • Design data collection tools in collaboration with Research Coordinators.
  • Monitor subject progress and ensure adherence to study protocols.
  • Provide education to subjects regarding the study, its purpose, and potential risks.
  • Attend meetings and communicate regularly with research staff.

Qualifications

  • Current registration with the relevant nursing regulatory body.
  • Minimum of one year of clinical experience, preferably in Neurology or chronic disease management.

Skills and Competencies

Strong interpersonal, oral, and written communication skills are essential. The ability to maintain accuracy and attention to detail while working under pressure is crucial. Candidates should demonstrate the ability to work independently and collaboratively within a team environment, exercising discretion and diplomacy as needed.

Benefits

Details regarding benefits and compensation will be provided upon inquiry.

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