All site staff working on the RAMPART trial are required to undertake trial-specific training before completing any actions for the study. Training is provided by the RAMPART trial team during site initiation and additional training sessions are organised periodically to provide training for new staff or as a refresher - please email the RAMPART trial team (email@example.com) if you wish to attend one of these. Alternatively you can review the slides in the table below in your own time. Please follow the links to access the individual training sessions.
After competing training, the RAMPART Training Log should be signed and retained in your Investigator or Pharmacy Site File as evidence.
|Rationale and Trial Design||
Investigators, Research Nurses, Trial Coordinators, Data Managers
|Screening, Consent and Randomisation|
Research Nurses, Trial Coordinators, Data Managers
|Data Collection and CRF Completion|
|TransRAMPART Sample Collection|
|Drug Supply Management System||
Research Nurses, Trial Coordinators, Data Managers, Pharmacists, Pharmacy Technicians
Pharmacists, Pharmacy Technicians