**Description**

This is a hybrid position which requires 2-3 days onsite at our Ridgefield, CT campus.

Responsible for the review, regulatory assessment and prioritization of adverse event and other product related information submitted to the company from clinical trial investigators, health care professionals and consumers. Through collaboration with Risk Management (RM) Physicians, Study Coordination, Regulatory Affairs, Biostatistics and Data Science (BDS) and Clinical Operations, this position ensures that adverse event information regarding the company´s products is submitted to the appropriate business units and health authorities. The Triage Manager ensures that adverse event cases contain complete medical information and are processed in a timely manner for submission to authorities as per federal regulations. The Triage Manager requests additional information from adverse event reporters where necessary in order to provide a complete medical story for the ca...