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Recently posted jobs
Biotech • Pharmaceutical
Run, optimize, and scale immunoassay and cell‑based potency assays for engineered cell therapies. Manage reagents and cell culture workflows, transfer methods into operations, maintain instruments, ensure data integrity and trending, mentor peers, and translate analytical outcomes to support development and product characterization.
Biotech • Pharmaceutical
Manage receipt, accessioning, storage, inventory, and controlled handling of human biological samples for cell therapy clinical studies. Maintain LIMS records, support approved sample pulls, sample transfers/returns/destruction, cold-chain storage, and collaborate with Biobank, HBS, and Quality teams to ensure traceability and compliant record-keeping.
Biotech • Pharmaceutical
Field-based leader driving scientific engagement and KOL advocacy for the ATTR brand across the U.S. West. Partners with Medical, Brand, Sales, and Market Access to deliver compliant scientific exchange, surface field insights, lead regional/national initiatives, represent the brand at congresses, and use digital/CRM tools and analytics to improve engagement and inform strategy. Manages projects, vendor relationships, and cross-functional alignment.
Biotech • Pharmaceutical
Lead strategic relationships with national trade and channel partners to support market access and brand priorities. Develop and execute account plans, collaborate cross-functionally for launches and negotiations, use data and market insights to drive decisions, and manage channel, supply, and access challenges while supporting patient access and account performance.
Biotech • Pharmaceutical
Field-based medical lead partnering with market access to develop and execute payer engagement strategies for oncology products. Build relationships with payer key decision-makers, communicate clinical and economic value, inform market access strategy, and represent oncology payer expertise within cross-functional teams.
Biotech • Pharmaceutical
Lead country-level delivery of oncology clinical trials by directing local study teams (CRAs/CSAs), overseeing site selection, regulatory/ethics submissions, budgets, CTMS and eTMF setup, monitoring, risk management, and audit readiness to ensure timely, high-quality data and study completion.
