Remote Clinical Data & Safety Specialist

Medtronic; Lombardia; Remote; EUR 40,000 - 60,000; Full time

Job summary

Medtronic in Milano, Italy seeks a Clinical Safety Specialist to support design, data collection, and safety reporting for clinical trials. This role emphasizes collaboration with stakeholders and rigorous data management to ensure compliant, high-quality safety data across studies.

The position requires practical clinical data expertise and a solid educational background, with relevant experience in designing protocols and managing data in a regulated environment.

Qualifications

• Requires practical knowledge and demonstrated competence within job area typically obtained through advanced education combined with experience.
• Requires a Baccalaureate degree (or for degrees earned outside of the United States, a degree which satisfies the requirements and minimum of 2 years of relevant experience, or advanced degree with 0 years of experience).

Responsibilities

• Collaborates with various stakeholders on the design, documentation, testing and implementation of clinical data collection studies, and clinical data review.
• Design and implement 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 protocols for cross-project consistency and identifying standard Case Report Form (CRF) modules to meet objectives.
• Provide early strategic input on protocol design focused on safety and/or data management issues.
• Review and resolve data discrepancies for standardized data validation systems and procedures.
• Prepares reports of clinical trial studies for internal validation and cross validation studies.
• Reports out in compliance with Regulatory reporting requirements.

Job description

Medtronic in Milano, Italy seeks a Clinical Safety Specialist to support design, data collection, and safety reporting for clinical trials. This role emphasizes collaboration with stakeholders and rigorous data management to ensure compliant, high-quality safety data across studies.

The position requires practical clinical data expertise and a solid educational background, with relevant experience in designing protocols and managing data in a regulated environment.