Research Nurse

Sentara

Norfolk, VAFull-time

Behavioral Health Market Context

Apply Nowvia Sentara Careers

Job Description

ucted in conformance with the protocol guidelines, departmental standards, and good clinical practices set forth by federal regulations. Sound conduct of the clinical trial including recruitment, screening, enrollment and follow-up of eligible subjects according to protocol requirements. Maintenance of accurate and complete documentation of related regulatory documents. Participates in writing, presenting, and publishing results of studies. As the primary resource for the protocols, will act as liaison between the Investigators, the institutional review board (IRB), and the Sponsor.

Education:
• Bachelor of Science Nursing- BSN

Certification/Licensure:
• Virginia RN License Virginia or Compact/Multi-State Eligible.
• All Direct Care RN's required to have BLS within 90 days of hire.
• Specialty certification Certified Clinical Research Professional (SOCRA CCRP or ACRP-CP) or Certified Clinical Research Coordinator (CCRC) is required within 3 years of employment.

Experience:
• 2 years of nursing or research experience required.

Keywords: #ZIP, Critical Care nurse, Heart, Cardiac RN, Cath Lab Nurse, Monster, Talroo-Nursing, RN EP Lab

Qualifications

  • Bachelor of Science Nursing- BSN
  • Virginia RN License Virginia or Compact/Multi-State Eligible
  • All Direct Care RN's required to have BLS within 90 days of hire
  • Specialty certification Certified Clinical Research Professional (SOCRA CCRP or ACRP-CP) or Certified Clinical Research Coordinator (CCRC) is required within 3 years of employment
  • 2 years of nursing or research experience required
  • Keywords: #ZIP, Critical Care nurse, Heart, Cardiac RN, Cath Lab Nurse, Monster, Talroo-Nursing, RN EP Lab

Benefits

    Responsibilities

    • The Research Nurse manages and coordinates all aspects of conducting clinical trials, both clinically and administratively
    • Utilizes in-depth knowledge of protocol requirements to ensure that studies are properly conducted in conformance with the protocol guidelines, departmental standards, and good clinical practices set forth by federal regulations
    • Sound conduct of the clinical trial including recruitment, screening, enrollment and follow-up of eligible subjects according to protocol requirements
    • Maintenance of accurate and complete documentation of related regulatory documents
    • Participates in writing, presenting, and publishing results of studies
    • As the primary resource for the protocols, will act as liaison between the Investigators, the institutional review board (IRB), and the Sponsor


    More Jobs