The Clinical Research Associate ensures study commitments are met efficiently and on time at the country level while acting as the main contact with the study site
Job Summary
The Clinical Research Associate ensures study commitments are met efficiently and on time at the country level while acting as the main contact with the study site.
This role involves site selection, initiation, monitoring, and closure in compliance with international guidelines and AstraZeneca procedural documents.
AstraZeneca is committed to diversity, inclusion, and innovation to transform rare disease treatment and improve patient lives.
Matching Summary
The Clinical Research Associate ensures study commitments are met efficiently and on time at the country level while acting as the main contact with the study site.
Skills & Requirements
Must-have
Clinical study site monitoring
Knowledge of ICH-GCP guidelines
Risk Based Quality Management
Clinical Monitoring Plan adherence
Study drug handling and data management
Travel flexibility up to 70%
Nice-to-have
Matrix reporting structure experience
Proactive communication skills
Ability to manage multiple tasks
Championing efficient clinical trial methods
Team-oriented and flexible
Experience with rare medical conditions
Key Requirements
Bachelor’s degree in life science or equivalent
Experience in clinical monitoring
Excellent knowledge of ICH-GCP and local regulations
Good medical knowledge and drug development understanding