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Medtronic
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Clinical Studies Spt Coord III -

Clinical Studies Spt Coord III -

4 - 9 years

|

10 - 14 Lacs

Posted:10 hours ago| Platform:

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Skills Required

training administration manager technology healthcare support services talent management individual contributor operations room supervision

Work Mode

Work from Office

Job Type

Full Time

Job Description

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

Requires minimum of 4 years of relevant experience .
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 of clinical study documents.
Assists with periodic audits of clinical study files for completeness and accuracy.

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