General Study Associate role supporting clinical trial delivery across BioPharmaceuticals Clinical Operations at AstraZeneca. Manages study documentation, regulatory compliance, vendor oversight, and administrative coordination throughout the clinical study lifecycle from setup through archiving.

Responsibilities

- Support Global Study Director and managers with delegated study work across multiple concurrent studies
- Initiate, maintain and close electronic Trial Master File ensuring ICH-GCP and SOP compliance
- Oversee non-critical path vendors for compliance with study requirements and processes
- Manage clinical regulatory documents and prepare administrative appendices for study reports
- Coordinate study logistics, materials,



supplies and administrative support during conduct and close-out

Requirements

- Education in medical, biological sciences, or clinical research discipline
- Proven organizational and analytical skills with attention to detail
- Previous administrative training or relevant experience
- Proficient computer skills for day-to-day work tasks
- Fluent English verbal and written communication
- Understanding of ICH-GCP guidelines and clinical study processes
- Ability to work independently and collaboratively in fast-paced environment

📌 Global Study Associate (España)
🏢 AstraZeneca
📍 España