Kelley Wilson

Kelley is a dedicated Regulatory Affairs professional with a wealth of experience spanning over 16 years in the pharmaceutical and food industries.

With a strong background in technical writing, Kelley is adept in filing complex regulatory submissions for new chemical entities and responding to authorities’ requests for information by interpreting and evaluating clinical study reports. Her previous roles, including Senior Manager of Medical Affairs and Associate Manager of Regulatory Affairs at Gilead Australia, have equipped her with comprehensive knowledge and skills in navigating the regulatory landscape.

In addition, Kelley brings expertise in both pharmacovigilance and clinical trial regulatory, quality and management activities. As Clinical Project Coordinator, Kelley brings together her technical, regulatory and project management skills to assist clients with novel therapies to understand the requirements to initiate clinical studies in Australia, New Zealand and internationally, including the USA.

Kelley is a great communicator and enjoys working in global team environments. She is based in New Zealand.