Job Summary

A medical technology company is filling a position for a Telecommute Senior Regulatory Affairs Specialist in Warwick.

Core Responsibilities of this position include:

• Preparing and submiting applications to the FDA
• Supporting in determination of the appropriate regulatory submission requirements and strategies
• Coordinating review of FDA submissions and test protocols

Required Skills:

• Ability and desire to travel as needed
• Knowledge and experience with regulatory requirements
• Good oral and written communications skills
• Working knowledge of statistics and electronic documentation and information systems