Clinical Data Spec

Medtronic; Varese; Sur place; EUR 65 000 - 90 000; Plein temps

Avantages offerts par ce poste

competitive salary

flexible benefits package

Medtronic Incentive Plan (MIP)

Résumé du poste

Medtronic in Italy seeks a Clinical Safety Specialist 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 discrepancies to support regulatory reporting.

Collaborate with stakeholders across projects to drive safety outcomes, ensure data integrity, and contribute to regulatory-compliant processes in a mission-driven healthcare company.

Qualifications

• 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.

Responsabilités

• 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.

Connaissances

communication

cross-functional collaboration

problem-solving

clinical data management

data collection systems

protocol design

Formation

Bachelor degree or equivalent with required experience

Description du poste

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