Position: Consultant - Scientific Affairs
Representing: Pharmaceutical Industry
Jessica has over 30 years' experience in the pharmaceutical industry in ethical companies working in a number of areas, including regulatory affairs, clinical research, medical information, medical devices, quality assurance & business development. Most recently, Jessica has specialised in a strategic role that involved in-licensing & business development, managing the Regulatory Affairs, Quality Assurance & Pharmacovigilance functions of Apotex to ensure the business imperatives of the company were met.
Jessica has been a member of the Electronic Distribution Working Group (EDWG) for the past 3 years, was the Chair of the GBMA Regulatory Working Group, a participant of the core group in the GBMA's Biologics Working Group & a representative in the Biosimilars Forum. She was integral in the development of the capstone subject for the Master of Pharmacy being run at UTS called Molecule to Market & is on the UTS Science Industry Advisory Group.
Jessica's goal is to see safe & effective medicines brought to market in the most effective & timely manner & is passionate about ensuring that patients can access current & accurate patient information in the most user-friendly manner utilising the latest technologies available.
