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. If the job isn’t quite right but you are looking for something similar, please get in touch. We also have multiple Temp, FTC, and Contract jobs available.
