About Your New Employer
Join a leading company in the healthcare industry in Galway. This company is looking for MDR Vigilance Specialists. This is a 12-month contract. You will oversee the company’s medical device surveillance program by evaluating adverse reports.
About Your New Job as a MDR Specialist
* You will oversee the company's drug or medical devices surveillance program, including intake, protocol development, evaluation, processing, and follow-up on adverse reports.
* Ensure 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, ensuring the creation of a unified database consistent with ADE standardization and internalization.
* Act as a liaison internally and with external collaborators to develop programs and processes to meet regulatory reporting requirements.
What Skills You Need as a MDR Specialist
* Bachelor’s degree in relevant field
* Knowledge within Medical device
* Strong communication skills
What’s on Offer as a MDR Specialist
* Entry level positions
* Good hourly rate
* Opportunity to work on diverse projects and develop specialized knowledge and skills
What’s Next
Apply now by clicking the “Apply Now" button or call us for more information.
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