Roche Cupido

At Tiervlei Trial Centre, I support the regulatory team with submissions and study start-up across allocated clinical trials. I authored the site's Work Instruction for regulatory clinical trial applications to SAHPRA, which was reviewed by the QA Lead.

I contribute to quality management planning and study-level risk assessments, and help prepare essential documents ahead of Site Initiation Visits. I also develop and validate eSource against protocol and CRF requirements.

I capture and reconcile participant data in Medidata Rave, maintain Investigator Site Files and participant/source files, and run weekly quality checks on study documentation. I prepare study and laboratory kits under supervision, working in line with GCP, study-specific SOPs, and regulatory standards.

Alongside my clinical research work, I tutored first-year mathematics at Stellenbosch University while completing a BSc in Human Life Sciences with Psychology. I’m interested in continuing to develop my skills and build a career in clinical research.