Clin Research Nurse Coordinator II - Neonatology

Job Summary

Coordinate all clinical research activities with minimal supervision. Assignments will include more complex studies that require a nurse’s clinical expertise.

Job Responsibilities

Expected to Perform all CRC Core responsibilities as detailed for CRNC I:

• Applies in depth knowledge of clinical research and coordinates conduct of complex studies..
• Manage study finances including sponsor invoicing & resolving study subject billing issues.
• Develop advertisement materials, informed consent document, Case Report Forms.
• Act as liaison for research subject, investigator, IRB, sponsor, and healthcare professionals.
• Document investigational product (drug/device) accountability.
• Self-monitor and self-audit responsibilities.
• Facilitate pre-study, site qualification,  study initiation, and monitoring visits.
• Facilitate study close out activities.
• Maintain Clinical Trial.gov /
• Assists other team members by educating, providing resources, and consulting on difficult protocols or projects.

• Understand  good clinical practice (GCP) and regulatory compliance Comply with Institutional, federal, state, and sponsor policies, standard operating procedures (SOPs) and guidelines.

Required Licenses, Certifications, Registrations

Required Education and Experience

Required Education: Bachelor of Science in Nursing (BSN) degree
 

Required Experience: Three (3) years of experience in nursing or research

Preferred Education, Experience & Cert/Lic

Preferred Licenses/certificates/registrations: ACRP or SOCRA

Additional Technical Requirements

Clinical Research Nurse responsibilities include but are not limited to CHOP mandatories and competencies for nurses, physical assessment, vital signs, administering investigational drugs and accessing lines for labs and pharmacokinetic sampling.