Assoc Clinical Data Spec

About Medtronic

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

Job Summary

A Day in the Life Responsibilities may include the following and other duties may be assigned.

Key Responsibilities

• 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.

Required Qualifications

• Requires broad theoretical job knowledge typically obtained through advanced education.
• 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).
• 0 years of experience required.

Benefits & Compensation

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.