About the Role
We are seeking an Assoc MDR Vigilance Specialist to join our team on a 12-month contract. This is a hybrid role, requiring 2 days of in-office work per week.
Responsibilities:
* Monitor the company's drug or medical devices surveillance program, including intake, protocol development, evaluation, processing, and follow-up on adverse reports.
* Participate in resolving legal liability and complying with government regulations.
* Maintain and report Medical Device Reports (MDRs), Adverse Drug Experience (ADE) data, or adverse reaction data as required by regulatory agencies.
* Analyze clinical databases for ADE data extraction and integrate it into a unified database, ensuring accuracy and quality of safety summaries.
Requirements:
* Bachelor's degree in Engineering, Science, Legal, Clinical, or related discipline.
* 1-2 years of experience in medical devices or related environments.
* Ability to think critically, make sound decisions, and work effectively in cross-functional teams.
* Strong attention to detail, knowledge of basic anatomy, physiology, and medical terminology.
* Patient safety and customer service focus, with high standards, operational excellence, accountability, and ethical behavior.
* Good communication skills and fluency in English, both written and spoken.