The Global Study Associate supports global clinical studies from set-up through close-out, ensuring compliance with clinical trial regulations and AstraZeneca policies
Job Summary
The Global Study Associate supports global clinical studies from set-up through close-out, ensuring compliance with clinical trial regulations and AstraZeneca policies.
AstraZeneca offers an inclusive environment with global career growth opportunities and encourages out-of-the-box thinking to accelerate growth and improve lives.
The role involves coordination of study activities, vendor oversight, regulatory submissions, budget tracking, and preparation of meetings and study documentation.
Matching Summary
The Global Study Associate supports global clinical studies from set-up through close-out, ensuring compliance with clinical trial regulations and AstraZeneca policies.
Skills & Requirements
Must-have
clinical study coordination
electronic Trial Master File management
regulatory document handling
study budget and payment tracking
clinical trial compliance
stakeholder collaboration
Nice-to-have
process improvement leadership
digitalization and Lean processes
cross-functional team communication
administrative and logistical support
Key Requirements
education in medical or biological sciences
experience in clinical research administration
proven organizational and analytical skills
computer proficiency
knowledge of ICH-GCP and clinical trial regulations