Marié van Wyk

Marié van Wyk brings 25 years of professional experience, including more than 12 years of clinical research industry experience to her role as FHI Clinical SA’s Global Head of Regulatory Affairs. She is responsible for global delivery of regulatory functions in alignment with the corporate strategy, policies, procedures and applicable regulations while maintaining the highest ethical, regulatory and scientific standards.

Her experience in regulatory affairs therapeutic areas includes an extensive range of indications and applications. The list of critical areas includes, but is not limited, to infectious diseases (including tuberculosis and HIV), oncology and vaccine trials (including COVID-19). Marié’s experience typically involves managing a clinical trial project from start-up to project completion. Her responsibilities include people management, trial management, budget management and customer interaction.

This regulatory affairs experience followed her extensive experience in various pharmacy environments as a retail pharmacist and hospital pharmacist in South Africa and the United Kingdom.

Marié not only holds a bachelor’s degree in Pharmacy from the North West University, South Africa but furthered her studies in the United Kingdom, where she obtained her MRPharmS (OSP) from Sunderland University. She also holds a management qualification from the Institute of Leadership & Management in the United Kingdom.