Publications

Project Manager

June 3rd, 2024

Published: June 3rd, 2024

Your responsibilities will include:

  • Assume overall responsibility for the preparation and maintenance of template documentation for study protocols, case report forms, informed consent forms, operational and regulatory documents, and other clinical research documentation as necessary.
  • Undertake participating site identification and recruitment
  • Assist in oversight of the study database, design and functionality, data quality and entry
  • Liaise with University of Melbourne Office of Research Ethics and Integrity regarding trial sponsorship and contracts.