Veeva Vault RIM Consultant - Managed Services

Slipstream Life Sciences

Pennsylvania

On-site

USD 120,000 - 150,000

Full time

14 days+
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Job summary

Slipstream is seeking a Veeva Vault RIM configuration expert to configure Vault objects, workflows, and security, while supporting data migration and integrations across Registrations, Submissions, and Publishing modules. You will work with regulatory teams to map eCTD requirements and ensure compliant, reliable environments for pharma and biotech clients.

The role covers implementing, migrating, and providing ongoing managed services with emphasis on quality, documentation, and client

Qualifications

  • Bachelor's degree in Life Sciences, Information Systems, Computer Science, or a related field.
  • 3-5+ years of hands-on Veeva Vault RIM configuration and/or administration experience.
  • Veeva Vault RIM certification strongly preferred.
  • Experience supporting at least one full RIM implementation, migration, or major upgrade lifecycle.
  • Experience with Vault release management and sandbox-to-production promotion processes.

Responsibilities

  • Configure and maintain Vault objects, lifecycles, workflows, and security matrices in Vault RIM.
  • Support data migration and bulk record management using Vault Loader, including data mapping and validation.
  • Configure RIM Registrations, Submissions, and Publishing modules per client requirements.
  • Manage release and environment activities, including UAT and sandbox-to-production promotions.
  • Triages and resolves Tier 2/3 client issues and documents configurations and SOPs.

Skills

Veeva Vault
RIM configuration
Data migration
Regulatory compliance
Client communication
Troubleshooting

Education

Bachelor's degree

Tools

Vault REST/SOAP
Vault Loader
SFTP
ERP integrations

Job description

Slipstream is seeking a Veeva Vault RIM configuration expert to configure Vault objects, workflows, and security, while supporting data migration and integrations across Registrations, Submissions, and Publishing modules. You will work with regulatory teams to map eCTD requirements and ensure compliant, reliable environments for pharma and biotech clients.

The role covers implementing, migrating, and providing ongoing managed services with emphasis on quality, documentation, and client

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