Clinical Studies Spcialist Coordinator II

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.

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.

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 of clinical study documents.

Document coordination - creates and manages the clinical study files and oversees the organization and distribution of clinical study documents.

Physical Job Requirements

• 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.
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Medtronic offers a competitive Salary and flexible Benefits Package

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