Jobs at AstraZeneca PLC

Leads Australian regulatory affairs for GMO-containing clinical trials and commercial products. Prepares DNIR and DIR submissions, coordinates scientifically robust packages, advises on OGTR and TGA requirements, supports clinical study start-up, monitors regulatory milestones and risks, and collaborates with global and local clinical, regulatory, biosafety, site, and consultant teams. The role focuses on cell and gene therapies and ensuring compliant approval pathways in Australia.

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

Lead full-cycle recruitment for a portfolio, design sourcing and attraction strategies, use talent intelligence tools (Eightfold), build talent pipelines, advise hiring managers, champion candidate experience, and develop capability in employer branding, hiring manager/candidate experience, or recruitment systems optimisation.

Support corporate communications by writing and publishing intranet stories, coordinating town halls, updating website content, preparing presentations and biographies, managing digital screen content, liaising with stakeholders, and providing general team support in a part-time fixed-term role.

Territory-based pharmaceutical sales role engaging GPs, pharmacies and allied health to educate on respiratory medicines, execute local sales strategy using data insights, meet territory targets, complete product training and Medicines Australia compliance.

Manage site activation, risk-based monitoring (remote and onsite), ensure patient safety and data integrity, coordinate regulatory/EC/IRB submissions, maintain CTMS/eTMF, conduct SDR/SDV/CRF review, report SAEs, manage study drug accountability, and produce monitoring reports to keep studies inspection-ready.

Lead and manage multiple high-profile clinical studies across all stages from feasibility to results. Drive cross-functional teams to deliver trials on time, on budget and to quality standards, ensure ICH-GCP and local regulatory compliance, and apply therapeutic-area knowledge within AstraZeneca's biopharma portfolio.