Clinical Research Nurse

6 days ago


Palo Alto, United States The Judge Group Full time

Our client is currently seeking a Research Nurse in Palo Alto, CA


Contract: 4-5 months


Overview:

seeking a Research Nurse 2, and will be under the direction of the principal investigator and/or research nurse manager, applying medical knowledge and experience to oversee and direct clinical course of research participants in clinical trials. Assess physical health and administer treatments throughout the study aligned with "Scope of Practice" delegated responsibilities. Oversee study conduct and ensure study participant safety.


This job will have the following responsibilities:

  • Ensure the safety of study participants, and maintain communication with their families/caregivers and clinicians.
  • Provide clinical and administrative nursing support and oversight for research clinical trials based on scope of practice. Collaborate with clinical staff, researchers, outside vendors, and other staff to administer treatment and study protocols. May coordinate multi-site studies.
  • Develop and manage budget for research study, and oversee resources including funds, personnel, and equipment as needed. Coordinate and collaborate with principal investigator to review study protocol and assess and analyze feasibility, budget projections, and staffing needs.
  • Conduct study participant evaluations according to the study protocol, assess adverse events, and apply triage and judgment to determine course of action.
  • Oversee and potentially administer medications and treatments per study protocol for out study participant research participants.
  • Comply with institutional policies, standard operating procedures, and guidelines, and prepare and submit documentation as required by the study protocol, study sponsor, and regulatory authorities. Interpret complex protocols and regulatory requirements. .
  • Supervise non-clinical research staff as needed.
  • Identify, recruit, and enroll study participants, as well as maintain study participant records and determine study participant criteria.
  • Host external audits (Food and Drug Administration, National Institutes of Health, etc.).
  • Support sponsor investigator research with Investigational New Drug/Investigational Device Exemption applications.


Qualifications & Requirements:

  • Bachelor's degree in nursing or equivalent
  • Five years of experience in nursing, with at least two years in a research setting.
  • Current license as a California Registered Nurse.
  • Certified Research Administrator or Clinical Research Coordinator preferred.
  • Current basic CPR certification.


Working Conditions:

  • May be required to work with, take specific precautions against, and/or be immunized against potentially hazardous agents.
  • May be exposed to blood borne pathogens.
  • On call 24 hours/day.
  • Frequent travel, might include international travel.


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