The Clinical Research Associate plays a key role in delivering clinical studies at allocated sites, ensuring study commitments are met efficiently and on time
Job Summary
The Clinical Research Associate plays a key role in delivering clinical studies at allocated sites, ensuring study commitments are met efficiently and on time.
This role involves close collaboration with various internal teams and requires monitoring, initiation, and closure of clinical study sites in compliance with international and local regulations.
AstraZeneca is committed to diversity, inclusion, and innovation in rare disease treatment, fostering a collaborative and ethical work environment.
Matching Summary
The Clinical Research Associate plays a key role in delivering clinical studies at allocated sites, ensuring study commitments are met efficiently and on time.
Skills & Requirements
Must-have
Clinical study site monitoring
ICH-GCP compliance
Risk Based Quality Management
Clinical Monitoring Plan adherence
Study drug handling and data management
High travel flexibility up to 70%
Collaboration with internal stakeholders
Nice-to-have
Matrix reporting structure experience
Proactive issue resolution
Championing process efficiencies
Multi-task prioritization skills
Technology impact understanding
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 understanding of drug development