Veeva Vault CTMS (Clinical Trial Management System) Consultant (RARR Job 5447)

We are seeking an experienced Veeva Vault Consultant with deep expertise across multiple Vault applications, including: The ideal candidate should have hands-on experience in Vault configuration, integration, validation, and migration, with a strong understanding of Life Sciences business processes and regulatory compliance.

Veeva Vault CTMS (Clinical Trial Management System)

· Strong technical knowledge of Configurations in Veeva Vault Clinical Operations Suite mainly in Veeva CTMS & Veeva eTMF

· Understand business requirements, and propose and design Tech solutions

· Configure and maintain clinical study workflows (Study, Country, Site).

· Experience in Clinical Trial data and processes across pharmaceuticals specifically as they relate to Clinical studies,

· Enable investigator management, site monitoring, visit tracking, and trip reporting.

· Support sponsor/CRO collaboration and study milestone tracking.

· Integrate CTMS with Vault eTMF or external systems for data consistency

· Work with Veeva technical team for issues or new features related to Veeva Vault ClinOps product

· Manage change requests, configuration, and enhancements in Vault application

· Assess the impact for periodic upgrades and support on implementing all upgraded features. All vault modules get upgraded with new releases 3 times a year.

· Guiding business decisions and priorities when proposing resolution strategies for encountered issues

· Experience with supporting ticketing systems like ServiceNow, Jira, etc. Experience in working on L2 support.

· Experience in ITIL process