Overview
As a Clinical Safety Specialist at Medtronic, you’ll collaborate to design, document, and implement clinical data collection studies and safety-focused data review. You will develop protocols and data systems, organize data for analysis, and resolve data discrepancies to support regulatory-compliant reporting. Your input will shape protocol design and data management across projects, driving safety outcomes and cross-functional collaboration. This role offers autonomy within a mission-driven company that prioritizes patients and healthcare innovation. You will contribute to advancing safe, data-driven medical technologies at scale.
Retribuzione / Benefits competitive salary
flexible benefits package
Medtronic Incentive Plan (MIP)
Responsabilità Collaborates with stakeholders on design, documentation, testing and implementation of clinical data collection studies and data review
Designs and implements 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 cross-project protocol consistency and identifying standard CRF modules
Provides early strategic input on protocol design focused on safety and/or data management
Reviews and resolves data discrepancies for standardized data validation systems and procedures
Prepares reports of clinical trial studies for internal and cross-validation
Reports in compliance with regulatory reporting requirements
Requisiti fondamentali Requires practical knowledge and competence in the job area
Bachelor degree (or equivalent with required experience) with minimum 2 years relevant experience, or advanced degree with 0 years
Experience likely obtained through advanced education and professional practice
communication
cross-functional collaboration
problem-solving
clinical data management
data collection systems
protocol design

📌 Clinical Data Spec (Milano)
🏢 Medtronic
📍 Milano