Description:
Main purpose of the job:To perform day to day of research related activities including but not limited to administration, laboratory activities, data collection, quality control, quality assurance, community recruitment and retention activities and ensuring compliance with regulatory and good clinical practice requirements within Research Centre studies at Wits RHI Location:
7 Esselen Street, Hillbrow, Wits RHI Research Centre Clinical Research Site (CRS) Key performance areas:
Assist Medical Technician or Medical Technologist with stock control and monitoring for all studies Ensure timeous and logical filling of shipment documents, Lab meeting minutes, and any other lab documents Capture, store, and ship samples on LDMS for study related protocols Assist Regulatory Officers/Managers, Sponsors / Monitors before, during and after monitoring visits Support Reg Officer/Managers to maintain regulatory files and filing systems Document regulatory team meetings as and when required Ensure staff are compliant to timely GCP training and renewals through active review of trackers and bookings as requires Review and support the Regulatory Officer/Manager and ensure that the study has all essential regulatory documentation filed and tracked on excel trackers Updating tracking logs for all submissions, approvals Promote studies and recruit participants by conducting presentations, radio talks and distributing brochures at the community Address potential participants in accordance with recruitment targets and participant recruitment standard operating procedures (SOP) Inform willing participants that participation in the study is voluntary Conduct screening interviews to consenting participant to determin
27 Jan 2026;
from:
gumtree.co.za