Clinical Data Spec
Pubblicato il 12-10-2026 - Medtronic in Firenze
A Day in the Life Business title will be Clinical Safety Specialist. Responsibilities may include the following and other duties may be assigned.
- 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 time is spent delivering and overseeing the projects – from design to implementation - while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education.
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DIFFERENTIATING FACTORSAutonomy: Established and productive individual contributor. Works independently with general supervision on larger, moderately complex projects / assignments. Organizational Impact: Sets objectives for own job area to meet the objectives of projects and assignments. Contributes to the comp