Jobs at AstraZeneca PLC

Lead strategic account planning and sales for lung oncology in Victoria, engage multidisciplinary hospital teams on approved indications, build senior stakeholder partnerships, run educational programs, and share insights across functions to drive on‑label prescribing and market access.

Territory-based pharmaceutical sales role partnering with GPs, pharmacies and allied health to promote CVRM medicines. Build relationships, execute local sales strategy, use data insights, complete product and Medicines Australia training, and ensure compliance with MA Code of Conduct while meeting sales targets and supporting patient outcomes.

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.

Lead end-to-end oncology study site start-up in Australia: manage HREC/RGO/TGA submissions, negotiate site contracts and budgets (FMV-aligned), drive activation readiness, maintain TMF and tracking systems, ensure ICH-GCP and local regulatory compliance, and implement process improvements to meet timelines and KPIs.

Territory-based GP Sales Representative for AstraZeneca's Respiratory unit on the NSW Central Coast. Build relationships with GPs, pharmacies and allied health; educate on approved medicines, execute local sales strategy, use data insights to tailor approaches, meet sales targets, complete product training and obtain Medicines Australia qualification while ensuring MA Code compliance.

Manage and lead cross-functional teams to deliver oncology clinical trials from feasibility through results. Oversee study timelines, budgets, quality, and compliance with ICH-GCP and local regulations. Provide project management, clinical study oversight, and stakeholder communication on high-profile studies during a 12-month contract.

Manage site activation and performance for oncology and cell therapy trials. Conduct remote and onsite monitoring (SDR/SDV/CRF), oversee regulatory submissions and document readiness, maintain CTMS/eTMF, report SAEs, apply RbQM to prioritize monitoring, and coach sites for inspection readiness.