Coordinate study activities from start-up to close-out
Maintain local etmf and isf
You'll provide technical expertise and support for the administrative aspects of clinical trials, ensuring each study meets its objectives with adequate resources while adhering to methodology standards
Job Summary
You'll provide technical expertise and support for the administrative aspects of clinical trials, ensuring each study meets its objectives with adequate resources while adhering to methodology standards.
Assist in the coordination and administration of study activities from start-up to execution and close-out within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost, and quality objectives.
At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit.
Matching Summary
You'll provide technical expertise and support for the administrative aspects of clinical trials, ensuring each study meets its objectives with adequate resources while adhering to methodology standards.
Skills & Requirements
Must-have
Technical expertise for administrative aspects
Coordinate study activities from start-up to close-out
Maintain local eTMF and ISF
Ensure timely document uploads for eTMF readiness
Coordinate administrative tasks during audits and inspections
Nice-to-have
Collaborate with various departments globally
Provide solutions to study conduct issues
Empowered to push boundaries of science
Inclusive culture championing diversity and collaboration
Key Requirements
Bachelor’s Degree preferred
Knowledge of relevant legislation and new developments in clinical development
Experience within the pharmaceutical industry
Experience in supporting clinical trials and study development