Clinical Data & Safety Specialist

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

Benefits offered by this job

Incentive Plan (MIP)

Job summary

Medtronic is seeking a Clinical Safety Specialist to collaborate with cross-functional teams on designing and implementing clinical data collection studies and protocols. The role focuses on safety and data management, with oversight of data quality, reporting, and regulatory compliance.

Typical responsibilities include resolving data discrepancies, preparing trial reports, and contributing to protocol design.

Qualifications

• Requires practical knowledge and demonstrated competence within job area typically obtained through advanced education and experience.
• Design and implement clinical protocols and data collection systems.
• Review and resolve data discrepancies for standardized data validation systems and procedures.

Responsibilities

• Collaborates with stakeholders on design, documentation, testing and implementation of clinical data collection studies and data review.
• Prepares reports of clinical trial studies for internal validation and cross validation studies.
• Reports out in compliance with regulatory reporting requirements.

Skills

Data management

Data analysis

Protocol design

Regulatory reporting

Education

Bachelor's degree

Job description

Medtronic is seeking a Clinical Safety Specialist to collaborate with cross-functional teams on designing and implementing clinical data collection studies and protocols. The role focuses on safety and data management, with oversight of data quality, reporting, and regulatory compliance.

Typical responsibilities include resolving data discrepancies, preparing trial reports, and contributing to protocol design.