We are looking for an experienced Veeva CTMS Specialist with solid hands-on expertise in managing Clinical Trial Management Systems (CTMS) and clinical trial data using Veeva / Veeva Vault CTMS .
Key Responsibilities
Manage and maintain clinical trial activities within Veeva CTMS .
Manage, update, track, and control clinical trial data in Veeva .
Handle CTMS activities across different stages of the clinical trial lifecycle .
Ensure CTMS data accuracy, completeness, and timely updates.
Coordinate directly with US/European client teams and internal stakeholders.
Support trial tracking,
documentation, reporting, and operational CTMS requirements.
Mandatory Requirements
Minimum 5+ years of hands-on CTMS experience .
Solid experience with Veeva CTMS / Veeva Vault CTMS .
In-depth experience managing clinical trial data within Veeva .
Experience independently managing and controlling CTMS activities for clinical trials.
Experience working directly with US or European clients .
Excellent verbal and written communication skills.
Comfortable working permanently in a US shift .
Delhi NCR candidates preferred.
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