Clinical Data Spec
Pubblicato il 14-10-2026 - Medtronic in Varese
h3Overview /h3pAs 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.
/ph3Retribuzione / Benefits /h3ullicompetitive salary /liliflexible benefits package /liliMedtronic Incentive Plan (MIP) /li /ulh3Responsabilità /h3ulliCollaborates with stakeholders on design, documentation, testing and implementation of clinical data collection studies and data review /liliDesigns and implements clinical protocols and data collection systems /liliDevelops systems for organizing data to analyze, code,
identify and report data and trends /liliManages data management issues by reviewing cross-project protocol consistency and identifying standard CRF modules /liliProvides early strategic input on protocol design focused on safety and/or data management /liliReviews and resolves data discrepancies for standardized data validation systems and procedures /liliPrepares reports of clinical trial studies for internal and cross-validation /liliReports in compliance with regulatory reporting requirements /li /ulh3Requisiti fondamentali /h3ulliRequires practical knowledge and competence in the job area /liliBachelor degree (or equivalent with required experience) with minimum 2 years relevant experience, or advanced degree with 0 years /liliExperience likely obtained through advanced education and professional practice /li /ulullicommunication /lilicross-functional collaboration /liliproblem-solving /liliclinical data management /lilidata collection systems /liliprotocol design /li /ul #J-*****-Ljbffr