Req #: 0000205783
Category: Professional / Management
Status: Per Diem
Shift: Day
Facility: Cooperman Barnabas Medical Center
Department: Cancer Ctr-Research

JOB SPECIFIC REQUIREMENTS

• Actively participates in ongoing research specific quality assurance activities such as chart audits for protocol compliance
• Conducts the informed consent process
• Coordinates shipping of blood, tissue samples, or pathology slides as required by clinical trial
• Coordinates the initiation and activation of all new clinical trial protocols,
• This includes, but is not limited to, verifying Scientific Review Board SRB, Institutional Review Board IRB and data collection plans prior to study activation
• Develops study tools including but not limited to study binders, medication diaries, eligibility checklists and flow sheets as required
• In collaboration with the physician, reviews patients’ charts and medical history to confirm protocol eligibility and obtains source documents i,e, medical record documentation as needed
• Maintains research record e,g, patient consent, eligibility, Case Report Forms CRF, registration confirmation, corresponding source documents, etc. for all patients enrolled in clinical trials
• Registers consented research patients with study sponsor e,g,industry, NCI Cooperative group, etc, and inputs into Oncore clinical trials database maintained by Rutgers Cancer Institute of New Jersey
  RWJBarnabas Health is an Equal Opportunity Employe

Please refer the Job description for details