- job summary: The Clinical Evaluations Specialist manages regulatory documentation for MDR remediation and PPRRs, requiring expertise in clinical literature reviews, regulatory writing, and post-market surveillance. This role supports medical device life cycle management and collaborates with cross-functional teams. Foreign-trained ophthalmologists are encouraged to apply. This is a 6-month on-site contract in Duluth, GA, with the potential for extension.job summary: The Clinical Evaluations Specialist manages regulatory documentation for MDR remediation and PPRRs, requiring expertise in clinical literature reviews, regulatory writing, and post-market surveillance. This role supports medical device life cycle management and collaborates with cross-functional teams. Foreign-trained ophthalmologists are encouraged to apply. This is a 6-month on-site contract in Duluth, GA, with the potential for extension.
