[Hiring] Clinical Data Specialist @Medtronic

Role Description

Business title will be Clinical Safety Specialist. Responsibilities may include the following and other duties may be assigned:

• 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.

Qualifications

• Requires a Baccalaureate degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) and minimum of 2 years of relevant experience, or advanced degree with 0 years of experience.

Requirements

• Requires practical knowledge and demonstrated competence within job area typically obtained through advanced education combined with experience.

Benefits

• Medtronic offers a competitive Salary and flexible Benefits Package.
• A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.
• We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
• Pay range: Italy: 40,000.00 EUR - 60,000.00 EUR.
• This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).