51±¾É«

Sandra is a Certified Clinical Research Professional (CCRP) with a sound understanding of ICH-GCP. She is currently working with the HRI Clinical Research Support Unit as the Clinical Research Associate Feasibility and Study Start-up. Her role is part of the Health Research Board National Clinical Trial Office ( HRB NCTO) Feasibility Programme.

Sandra holds a Bachelor’s degree in Public Health from Monash South Africa and a MSc in Public Health from 51±¾É«. She has contributed to clinical trials by guiding regulatory processes to obtain ethics approval, developing study-specific SOPs, creating concise training materials, conducting site initiation visits, training study staff, developing, and maintaining ISFs/TMFs and general research administration.