Research Coordinator

Description:

• Administrative Research

  • Develop informed consent forms, source documents, worksheets and case report forms

  • Develop databases

  • Prepare and submit study documents to the ethic board

  • Retrospective chart review and perform data entry for studies

  • Complete case report forms and review them against the patient's medical record for completeness and accuracy

• Participant Management

  • Recruit eligible subjects for research projects

  • Obtain consent from subjects wishing to participant in health research projects according to standard approved protocol

  • Administering questionnaires or diaries per protocol

  • Monitoring research participants to ensure adherence to study rules

• Project Management

  • Ensuring compliance with SOPs and local regulations

  • Ensuring that the necessary supplies and equipment for a study are in stock and in working order

  • Collect and maintain data logs

  • Complete binders for prospective studies and clinical trials

  • Develop project timelines

• Communication and Coaching

  • Training other colleagues on protocol requirements, proper source documentation and case report form completion

  • Assist faculty member with the coordinating research staff and volunteers, including assisting with the delegation of tasks and duties

• Budget Management

  • Analyze budgets for agreements with sponsors

  • Prepare invoices for billing purposes for various research studies