Principal Regulatory Affairs Manager - Mettawa, IL

Only for registered members Mettawa, IL , United States

1 month ago

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Job summary

The Principal Regulatory Affairs Manager will lead global submission work for CDx trials and submissions to support product commercialization in multiple regions. They will mentor the organization on key activities and develop regulatory strategies for external partnerships and product lifecycle management.

Responsibilities

  • The Principal Regulatory Affairs is responsible for regulatory strategy development and execution for high-complexity diagnostics specifically Companion Diagnostics and digital pathology in the clinical oncology environment

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