Clinical Data & Safety Specialist

Medtronic; Milano; Presencial; EUR 40 000 - 60 000; Tempo integral

Resumo da oferta

Medtronic is seeking a Clinical Safety Specialist in Italy (Milano) to collaborate across stakeholders on designing and implementing clinical data collection studies and protocols. The role emphasizes safety-focused data management, analysis, and timely reporting for regulatory compliance.

Responsibilities include resolving data discrepancies, preparing trial reports, and ensuring alignment with regulatory standards while contributing to project milestones within a professional team.

Qualificações

• Requires practical knowledge and demonstrated competence within the clinical safety domain.
• Bachelor's degree with minimum 2 years of relevant experience, or an advanced degree with 0 years experience.

Responsabilidades

• Collaborates with stakeholders on design, documentation, testing and implementation of clinical data collection studies and data review.
• Designs and implements clinical data collection protocols and data systems.
• Develops systems for organizing data to analyze, code, identify and report data and trends.
• Reviews data discrepancies for standardized data validation systems and procedures.
• Prepares reports of clinical trial studies for internal validation and cross validation.
• Reports out in compliance with regulatory reporting requirements.

Formação académica

Bachelor's degree

Descrição da oferta de emprego

Medtronic is seeking a Clinical Safety Specialist in Italy (Milano) to collaborate across stakeholders on designing and implementing clinical data collection studies and protocols. The role emphasizes safety-focused data management, analysis, and timely reporting for regulatory compliance.

Responsibilities include resolving data discrepancies, preparing trial reports, and ensuring alignment with regulatory standards while contributing to project milestones within a professional team.