Clinical Research Associate - BioPharmaceutical

Ensure centrally managed study delivery at AstraZeneca by maintaining clinical study documents in the Global Electronic Library, coordinating with Data Management and Document Management teams, and monitoring administrative processes through audits and regulatory inspections. The role serves as technical owner within Patient Safety, tracks study materials and equipment, and identifies opportunities to improve clinical development methodology. A bachelor's degree in a relevant discipline and prior study management experience within a pharmaceutical or clinical background are required.