Clinical Data Spec
Pubblicato il 12-10-2026 - Medtronic in Milano
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