Role Description
Job is focused initially at report testing for reports / dashboards developed in tools like SQL, Spotfire, PowerBi, etc.
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Collaborates with various departments on the design, documentation, testing, and implementation of clinical data collection studies, and clinical database review.
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Design and implement clinical protocols and data collection systems.
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Develops systems for organizing data to analyze, identify and report data and trends.
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Manages data management issues by reviewing protocols for cross-project consistency, and identifying standard Case Report Form (CRF) modules to meet objectives.
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Develops data quality plans.
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Provide early strategic input into protocol design focused on data management issues.
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Review and resolve data discrepancies for standardized data validation systems and procedures.
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Prepares reports of clinical trial studies for internal validation and cross validation studies.
Qualifications
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Requires a Baccalaureate degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. Β§ 214.2(h)(4)(iii)(A) and minimum of 2 years of relevant experience, or advanced degree with 0 years of experience.
Requirements
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Requires practical knowledge and demonstrated competence within job area typically obtained through advanced education combined with experience.
Benefits
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Medtronic offers a competitive Salary and flexible Benefits Package.
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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.
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We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
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This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).