About Your New Job
As a Drug/Medical Device Surveillance Specialist, you will monitor the company’s surveillance program for adverse events related to drugs and medical devices.
You will ensure accurate intake, protocol development, evaluation, processing, and thorough follow-up of adverse reports, always meeting strict regulatory guidelines.
You will participate in the resolution of legal liabilities and assist with government regulatory compliance, including the preparation and reporting of Medical Device Reports (MDRs) and Adverse Drug Experience (ADE) data.
You will review and analyze clinical databases, extract ADE data, and integrate this information to uphold data accuracy and quality.
You will act as a liaison both internally and externally to support the development of effective programs and processes to meet regulatory reporting requirements.
Most of your time will be spent delivering and overseeing project work from start to finish, collaborating closely with other stakeholders.
What Skills You Need
Strong theoretical knowledge of the field, typically acquired through advanced education.
Excellent written and verbal communication skills, with the ability to work effectively in collaborative environments.
Attention to detail, data analysis experience, and organizational skills required to maintain high quality and compliance standards.
What's on Offer
Competitive salary package
Opportunity for professional growth in a specialized, high-demand area of healthcare.
Dynamic team environment, ongoing support and training opportunities.
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