Playing a critical role within Scholar Rock, the Associate Director/Director of Clinical Quality Audits will lead the Clinical Quality Audit Program, develop/implement processes and systems governing the Clinical Quality Audit Program activities and will report into the Senior Director of CQA.

The Sr. Regulatory Affairs Specialist is responsible for the preparation of regulatory submissions required to market new or modified medical devices and in vitro diagnostic devices in both domestic and international clinical markets. This entails development, execution and management of procedures and systems designed to ensure that the product development process addresses all regulatory requirements.