We are driving the next generation of discoveries to address critical cancer challenges and accelerate the translation of scientific evidence into patient benefit.
Fostering an outstanding cancer care workforce to help maintain and enhance world-leading patient outcomes through online learning, courses and events.
Investigator-initiated trials usually have a Data Manager within the Sponsor-Investigator’s central coordinating trial team.
Responsibilities may include:
Development of the Data Management Plan and any other SOPs or guidelines to ensure data management activities are in accordance with Good Clinical Practice (GCP) and any other applicable regulations or local requirements
Coordinate the design, build, test and validation of the Case Report Form (CRF) or clinical database
Coordinate process for integrating other systems for Electronic Data Capture (EDC)
Develop CRF Completion Guidelines for participating sites
Assign database user permissions in accordance with PI approval
Enter data from paper CRFs into database
Perform data cleaning, resolve data queries
Generate datasets for interim analysis (if applicable) or reporting and final analysis (after database lock)
Archive trial data at end of trial
See Data Management, for further information about activities.
Get the latest in cancer news, events and more, direct to your inbox
Join a network of Victorian cancer researchers, clinicians and consumers to keep your finger on the pulse.
