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Milano, Lombardia, Italy
Tempo pieno
R79175
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the Life
Business title will be Clinical Safety Specialist.
Responsibilities may include the following and other duties may be assigned.
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- Collaborates with various stakeholders on the design, documentation, testing and implementation of clinical data collection studies, and clinical data review.
- Design and implement clinical protocols and data collection systems.
- Develops systems for organizing data to analyze,
code, identify and report data and trends.
- Manages data management issues by reviewing protocols for cross-project consistency and identifying standard Case Report Form (CRF) modules to meet objectives.
- Provide early strategic input on protocol design focused on safety and/or data management issues.
- Review and resolve data discrepancies for standardized data validation systems and procedures.
- Prepares reports of clinical trial studies for internal validation and cross validation studies.
- Reports out in compliance with Regulatory reporting requirements.
SPECIALIST CAREER STREAM:
Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of tim
📌 Clinical Data Spec (Romano di Lombardia)
🏢 Medtronic
📍 Romano di Lombardia
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