Sharon Matshebele

Facilitated daily clinical trial operations for pharmaceutical- and CRO-sponsored haematology studies, collaborating with Clinical Research Coordinators and Principal Investigators to achieve 100% adherence to study timelines. Reviewed and reconciled source documentation for complex participant visits, reducing initial query generation by 27% through rigorous quality control before database entry.

Spearheaded stakeholder engagement across key hospital and clinical accounts, boosting HCP participation in compliance and therapeutic education initiatives by 35%. Captured, verified, and escalated adverse events and product quality complaints within mandatory 24-hour pharmacovigilance timelines, maintaining a 100% regulatory reporting compliance rate.

Managed scientific communication and product education across a designated hospital network, driving full therapeutic guideline adoption while maintaining 100% adherence to national pharmaceutical marketing codes and internal SOPs. Processed and documented serious adverse events and non-serious adverse drug reactions under rigorous pharmacovigilance protocols, consistently meeting regulatory submi

Trained as a medical sales representative, supporting pharmaceutical sales and customer engagement activities.

Conducted research activities supporting professional placement and recruitment operations.

Supported proposal development and documentation processes for consulting engagements.

Ongoing postgraduate diploma in public health.

Completed training in Good Clinical Practice (ICH-GCP).

Completed a qualification in pharmaceutical sales representation at NQF level 5.

Completed a business management qualification at NQF level 5.

Bachelor of Science degree with a double major in Biochemistry and Chemistry.

Completed training in ethics in health research.

Completed a course in clinical data management for clinical research via Coursera.

Completed a course in SQL for data science via Coursera.