The Clinical Research Associate (CRA) is responsible for the delivery of clinical studies at allocated sites and plays a key role in the local study team(s)
Job Summary
The Clinical Research Associate (CRA) is responsible for the delivery of clinical studies at allocated sites and plays a key role in the local study team(s).
This role involves the selection, initiation, monitoring, and closure of assigned sites in clinical studies, adhering to AstraZeneca Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations.
At AstraZeneca, we push the boundaries of science to transform complex biology into transformative medicines for rare diseases.
Matching Summary
The Clinical Research Associate (CRA) is responsible for the delivery of clinical studies at allocated sites and plays a key role in the local study team(s).
Skills & Requirements
Must-have
monitoring clinical studies
ICH-GCP knowledge
local regulations knowledge
site selection and initiation
study monitoring visits
essential document management
Nice-to-have
remote collaborator environment
positive change management
efficient process championing
prioritize multiple tasks
proactive communication
rare disease experience
Key Requirements
Bachelor’s degree or equivalent
Experience of monitoring
Demonstrates flexibility and willingness to travel