Clinical Trial Registries Associate - Irvine

Only for registered members Irvine, United States

2 weeks ago

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Job summary

The Clinical Trial Registries Associate is a member of the Global Clinical Trial Registries Team within Business Operations, part of Drug Development Operations.

Responsibilities

  • Provide support in quality oversight of the Registry health for studies within and across programs
  • Contribute to Registry submission activities
  • Provide guidance in global Registry requirements
  • Provide support for Registry submission process improvement activities

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