Jobs at AstraZeneca

Conducts early bioprocess research for preclinical vaccine candidates, including screening, optimization, lab-scale purification, characterization, formulation, and stability testing. Develops analytical assays, troubleshoots processes, documents findings for regulatory submissions and technology transfer, interprets data, and communicates recommendations. Maintains laboratory records, operates instruments, and collaborates with project teams and external vendors in an in-person laboratory environment.

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.

Conducts remote and onsite monitoring for clinical trial sites, including site qualification, study start-up, risk-based monitoring, source data review, safety reporting, investigational product accountability, recruitment tracking, compliance, and inspection readiness. Maintains CTMS and eTMF records, resolves data queries, prepares monitoring reports, and collaborates with investigators and cross-functional study teams to ensure participant safety, data quality, and timely study delivery.

Supports clinical study start-up activities from site selection through activation. Maintains tracking spreadsheets, logs, communication tools, and essential study documents; reviews Sub-Investigator and regulatory documentation; processes vendor access; monitors document workflows and activation risks; and provides status updates in study team meetings. The role follows ICH-GCP, company procedures, and applicable regulations while supporting timely, compliant, and cost-effective site activation.

Provides national leadership for AstraZeneca’s field-based Clinical Trial Liaison team. Develops strategy, manages performance and talent, coordinates engagement with research sites and investigators, and partners with Medical Affairs, R&D, Clinical Operations, and Brand teams. Uses field insights to improve study planning, trial execution, patient recruitment, and access to innovative medicines. Ensures scientific rigor, compliance, operational discipline, and effective cross-functional collaboration across prioritized US clinical studies.

Lead country-level clinical study start-up activities, including site activation, regulatory and ethics submissions, informed consent review, language negotiations, feasibility planning, documentation, and eTMF readiness. Serve as the primary site contact, maintain CTMS data integrity, monitor milestones and risks, and collaborate with clinical operations teams, CRAs, vendors, ethics committees, and health authorities to accelerate study activation and support compliant trial delivery.

Leads and coaches a regional Clinical Trial Liaison team supporting strategic clinical research sites across the US. Translates national priorities into regional field plans, strengthens investigator and site engagement, accelerates trial start-up and enrollment, communicates field insights, and partners with Medical Affairs, Clinical Operations, and site management teams. Oversees performance, talent development, resources, compliance, travel, and change adoption while ensuring alignment with FDA requirements and AstraZeneca policies.

Leads and coaches a regional Clinical Trial Liaison team supporting investigator and research-site engagement across US clinical trials. Translates national priorities into regional field plans, improves trial start-up, enrollment, and retention, and coordinates with Clinical Operations, Site Management, Medical Affairs, MSLs, and other partners. The role manages talent, performance, resources, travel, compliance, and field insights while driving execution, change adoption, and scientific engagement across AstraZeneca’s clinical pipeline.

Educates healthcare professionals on respiratory medicines, clinical evidence, approved indications, and safety profiles to support appropriate prescribing. Manages a designated sales territory by developing business plans, analyzing market and managed care information, implementing strategic targeting plans, leveraging promotional resources, and meeting sales forecasts and budgets. Provides compliant educational programs, coordinates with other sales specialists, completes product training, and builds strong healthcare-provider relationships.

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.