We are looking for an experienced Veeva CTMS Specialist with strong 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.
- Robust 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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