Global Study Associate – 12 Month Contract

AstraZeneca seeks a Global Study Associate to support delivery of clinical studies within BioPharmaceuticals Clinical Operations.

Responsibilities

• Support GS(A)D and GSMs by completing delegated study work, potentially across multiple studies and delivery models concurrently.
• Initiate and lead the set‑up of the electronic Trial Master File (eTMF) and maintain it through close‑out to ensure compliance with ICH‑GCP and AstraZeneca SOPs.
• Collect and manage regulatory and other essential documents, collaborating with internal staff and external stakeholders.
• Create and manage clinical regulatory documents in ANGEL, ensuring technical standards are met for effective submission to regulatory authorities.
• Plan and collate administrative appendices for the CSR.
• Generate study documents, ensuring template and version compliance per study requirements.
• Populate and...