Veeva RIM Consultant

Job Description:

• Implement, configure, and support Veeva Vault RIM applications.
• Support regulatory submissions, product registrations, and regulatory lifecycle management.
• Gather business requirements and collaborate with Regulatory Affairs and IT teams.
• Manage regulatory data, workflows, system enhancements, and UAT.
• Ensure compliance with pharmaceutical regulatory processes and GxP requirements.

Required Skills:

• Hands-on experience with Veeva Vault RIM.
• Strong understanding of Regulatory Affairs and Regulatory Operations.
• Experience with Registrations, Submissions, and regulatory data management.
• Knowledge of eCTD, GxP, and global regulatory processes.
• Excellent analytical and communication skills.
• Experience: 5+ years in pharmaceutical regulatory systems or relevant Veeva RIM experience.

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