Clinical Data Specialist

Medtronic

1d

About The Position

This job is focused initially at report testing for reports/dashboards developed in tools like SQL, Spotfire, PowerBi, etc. Collaborates with various departments on the design, documentation, testing, and implementation of clinical data collection studies, and clinical database review. Design and implement clinical protocols and data collection systems. Develops systems for organizing data to analyze, 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. Develops data quality plans. Provide early strategic input into protocol design focused on 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. SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects – from design to implementation - while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education.

Requirements

• 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 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.

Nice To Haves

• report testing for reports / dashboards developed in tools like SQL, Spotfire, PowerBi, etc.

Responsibilities

• Design and implement clinical protocols and data collection systems.
• Develops systems for organizing data to analyze, 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.
• Develops data quality plans.
• Provide early strategic input into protocol design focused on 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.

Benefits

• competitive Salary
• flexible Benefits Package
• Medtronic Incentive Plan (MIP)

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level