Profile

Well-rounded Consultant Clinical Research Associate and Project Manager with over 13 years of experience in clinical research across both pharmaceutical companies and CROs.
Expertise spans start-up activities, regulatory and ethics submissions, site and project management, study plan development, team leadership, and training. Therapeutic experience includes Phase II–III trials in oncology, CNS, pain, cardiovascular, infectious disease, endocrinology, gynaecology, vaccines, medical devices, and pulmonology.

Proven track record in navigating sponsor and regulatory audits and inspections. Highly skilled in clinical trial planning, cross-functional collaboration, and building strong stakeholder relationships. Results-oriented with excellent communication, organizational, and problem-solving abilities, with a strong aptitude for leading and influencing change.
Holds a BTech in Pharmaceutical Sciences and Biomedical Technology from Tshwane University of Technology and completed Practical Project Management through UNISA School of Business Leadership