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Clinical Research Nurse Coordinator I
Ref No.: 18-14053
Location: Philadelphia, Pennsylvania
Coordinate all clinical research activities with moderate supervision. Assignments may include more complex studies that require a nurse's clinical expertise.

Responsibilities:
Expected to Perform all CRC Core responsibilities (as applicable):
  • Adhere to an IRB approved protocol
  • Coordinate protocol related research procedures, study visits, and follow-up care
  • Participate in the informed consent process of study subjects, screen, recruit and enroll patients/research participants
  • Support the safety of clinical research patients/research participants
  • Educate subjects and family on protocol, study intervention, study drug, etc.
  • Facilitate pre-study, site qualification, study initiation, and monitoring visits
  • Facilitate study close out activities
  • Coordinate research/project team meetings
  • Maintain study source documents and regulatory documents
  • Report adverse events
  • 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
RN License, CPR Certification

Required Education and Experience
Required Education: ASN/BSN
Required Experience: 1+ years nursing/research
Preferred Licenses/certificates/registrations: ACRP or SOCRA

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.