The Reporting Specialist I is responsible for executing all of the reporting, in partnership with internal and
external stakeholders. The individual will also partner with internal teams such as pharmacovigilance, local incountry
teams, and the device quality assurance team to ensure the appropriate and accurate reporting of
complaints. They will interface with regulators and serve as the liaison to the respective team when questions
and requests arise.

Responsibilities 

• Decision maker for reportability decisions
• Lead for all vigilance reporting, including local and global submissions
• Partners with pharmacovigilance, regulatory affairs, in-country teams, and device QA for submissions and escalates requests as appropriate
• Ensures that relevant stakeholders have visibility to the reporting and where they are in the process
• Manages regular reporting needs and external requests (i.e. from the FDA)
• Manage the timeline for end to end reporting
• Owns translation services for reporting