Conduct participant recruitment, screening, informed consent, and randomization/re- randomization
Data collection, data entry, documentation, and organization per the study protocol and standard operating procedures
Site stock management
Send daily site reports
Communicate regularly with the Study Coordinators and other study staff and will respond to data and study queries with information and reports as required
Assist caregivers and adolescents with disclosure support
Maintain study registers, logs, and files and make sure all study documents are kept secure and locked
Write reports and participate in study meetings as require