Assoc MDR/Vigilance Spec
710 Medtronic Parkway Mounds View, MN 55432 US
Job Description
Top 3 things the manager is looking for:Â
- MDR Experience
- Previous healthcare experience
- Med device company experience
Top 3 Tasks in Scope for this role:Â
- Review incoming complaints from the field
- Go back out to the field for further information on complaints
- File regulatory reports
• Monitors the company's drug or medical devices surveillance program including the intake, protocol development, evaluation, processing, and follow-up on adverse reports, participation in the resolution of any legal liability and in complying with government regulations.
• Ensures complete and accurate maintenance and reporting of Medical Device Reports (MDRs), Adverse Drug Experience (ADE) data or adverse reaction data as required by regulatory agencies.
• Review and analyze clinical databases for the extraction of ADE data and integrates the data to ensure the creation of a unified database consistent with the aims and purposes of ADE standardization and internalization as well as to ensure the accuracy and quality of safety summaries.
• Acts as a liaison internally and with external collaborators to develop programs and processes to meet regulatory reporting requirements.
Must Have: Minimum Requirements
• Bachelors degree required
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