Minimum two years clinical study monitoring experience
Funds knowledge of ich-gcp guidelines
This role involves monitoring clinical studies in various oncology therapeutic areas to ensure data accuracy and timely reporting
Job Summary
This role involves monitoring clinical studies in various oncology therapeutic areas to ensure data accuracy and timely reporting.
The position requires active participation in all study phases from feasibility and setup through closure, including center selection and recruitment support.
AstraZeneca offers a diverse, inclusive work environment committed to sustainability and providing opportunities for lifelong learning and career development.
Matching Summary
This role involves monitoring clinical studies in various oncology therapeutic areas to ensure data accuracy and timely reporting.
Salary
Not specified; Not specified; Not specified
Skills & Requirements
Must-have
Completed natural science or medical degree
Minimum two years clinical study monitoring experience
Funds knowledge of ICH-GCP guidelines
Experience with electronic data capture systems
Willingness to travel extensively within DACH region
Nice-to-have
Interest in Risk Based Quality Management approaches
Experience with Remote Monitoring methodologies
Strong analytical and solution-oriented thinking
Fluency in English language
Ability to work independently and structured
Key Requirements
Natural science or medical university degree
At least two years as a monitor in clinical studies
Secure handling of legal and regulatory requirements (AMG)
Travel readiness for overnight stays across Germany, Austria, and Switzerland