Medtronic
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Clinical Studies Specialist Coordinator II
Description
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.
**A Day in the Life**
**Responsibilities may include the following and other duties may be assigned.**
**Supports clinical studies by executing and maintaining one or more of the following areas.**
**Data coordination- actively participates in the development and testing of case report forms, study reports, and study databases based on protocol requirements.**
**Ensures timely and quality completion of data forms, verifies study data, and generates, manages and resolves data discrepancies.**
**May process compensation & identify and resolve compensation discrepancies.**
**Document coordination - creates and manages the clinical study files and oversees the organization and distribution...
**A Day in the Life**
**Responsibilities may include the following and other duties may be assigned.**
**Supports clinical studies by executing and maintaining one or more of the following areas.**
**Data coordination- actively participates in the development and testing of case report forms, study reports, and study databases based on protocol requirements.**
**Ensures timely and quality completion of data forms, verifies study data, and generates, manages and resolves data discrepancies.**
**May process compensation & identify and resolve compensation discrepancies.**
**Document coordination - creates and manages the clinical study files and oversees the organization and distribution...