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Veeva RIM Specialist

ImmunityBio

Summit, New Jersey, United States Full time June 26, 2026
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Vacancy Description

Position Summary

The Veeva RIM Specialist will provide expertise and guidance in the management and publishing of regulatory documents ensuring their conformance with Health Authority requirements. This role is hands on and execution focused, working closely with all of regulatory affairs to support all US and ex-US regulatory activities and maintain inspection-ready system. This position will assist staff in submission and document management activities using Veeva RIM software.

Essential Functions

  • Create and maintain electronic project folders for projects.
  • Execute the upload, tracking, life cycle maintenance of regulatory submissions, including INDs, BLAs, CTAs, for US and ex-US regions within Veeva RIM.
  • Maintain Veeva RIM by uploading all submissions, Health Authority correspondence, etc.
  • Track all regulatory meetings, questions, information requests, and responses ensuring proper linking within Veeva RIM. Upload a...
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