Teams at AstraZeneca

Leads Australian regulatory affairs for GMO-containing clinical trials and commercial products. Prepares DNIR and DIR submissions, advises on OGTR requirements and approval pathways, coordinates scientifically robust regulatory packages, monitors application milestones and risks, and collaborates with clinical teams, sites, IBCs, consultants, TGA, OGTR, and global regulatory experts. Supports cell and gene therapy development, clinical trial start-up, compliant GMO dealings, and product registration or lifecycle activities.

Promote AstraZeneca respiratory medicines to GPs, pharmacies, and allied health professionals across Sydney’s North Shore and Northern Beaches. Build healthcare partnerships, educate customers on approved medicines, execute territory sales strategies, use data to understand customer needs, achieve sales targets, complete Medicines Australia training, and maintain compliance with the MA Code of Conduct.

Provide technical support and troubleshooting for QC laboratory instruments, lead validation and decommissioning projects to GMP/GLP standards, administer Empower software, author and maintain protocols/SOPs, coordinate vendor servicing and calibrations, perform routine maintenance and ad hoc testing, and drive continuous improvement and data integrity.