At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe
Job Summary
At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe.
The Senior Analyst I, Clinical Trial Safety is responsible for tools set-up, scripting, and data analysis tasks for the Clinical Trial Safety, working closely with Analysts and Scientists to ensure safety data deliverables meet quality and timelines.
AstraZeneca is an equal opportunity employer committed to diversity and inclusion and providing a workplace free from discrimination, with accommodations available for persons with disabilities.
Matching Summary
At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe.
Skills & Requirements
Must-have
Clinical trial safety data analysis
Data review tool setup and maintenance
Medical data completeness and accuracy
Clinical data visualization
Programming experience in data analysis
Knowledge of ICH/GCP guidelines
SAE reporting requirements
Nice-to-have
Cross-functional collaboration
Continuous improvement and training
Experience with JReview, JMP Clinical, Spotfire
Statistic knowledge
Strong attention to detail
Ability to summarize complex information
Key Requirements
Bachelor degree in related discipline
Minimum 2 years clinical study experience
Understanding of clinical study and drug development
Knowledge of ICH/GCP Guidelines
Knowledge of SAE reporting requirements
Advanced computer skills including Microsoft Power Platform