Clinical Studies Specialist Coordinator II
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Key skills for this role
About the Role
Medtronic is seeking a Clinical Studies Specialist Coordinator II to support clinical studies by executing data coordination and document coordination tasks. The role involves developing case report forms, verifying study data, managing discrepancies, and organizing clinical study files.
Key Skills for This Role
Responsibilities
- Support clinical studies by executing and maintaining data coordination and document coordination areas
- Participate in development and testing of case report forms, study reports, and study databases
- Ensure timely and quality completion of data forms, verify study data, and manage data discrepancies
- Create and manage clinical study files and oversee organization and distribution of clinical study documents
- Assist with periodic audits of clinical study files for completeness and accuracy
Requirements
- Minimum 2 years of relevant experience
- Full job knowledge of systems and procedures obtained through prior work experience or education
Full Job Posting
A Day in the Life
- Supports clinical studies by executing and maintaining data coordination and document coordination.
Responsibilities
- Data coordination: actively participates in development and testing of case report forms, study reports, and study databases.
- Ensures timely and quality completion of data forms, verifies study data, and generates, manages and resolves data discrepancies.
- May process compensation and identify and resolve compensation discrepancies.
- Document coordination: creates and manages clinical study files and oversees organization and distribution of clinical study documents.
- Assists with periodic audits of clinical study files for completeness and accuracy.
Required Knowledge and Experience
- Requires full job knowledge of systems and procedures obtained through prior work experience or education.
- Requires minimum of 2 years of relevant experience.
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