We are looking for an experienced Veeva CTMS Specialist with strong hands-on experience in Clinical Trial Management Systems (CTMS) and managing clinical trial data using Veeva.
The candidate should have a robust understanding of clinical trial operations and should be capable of managing and controlling CTMS-related activities across clinical trials.
Key Responsibilities
- Manage and maintain Clinical Trial Management System (CTMS) activities.
- Work extensively on Veeva CTMS / Veeva Vault CTMS.
- Manage and maintain clinical trial data within Veeva.
- Ensure accuracy and completeness of clinical trial information in CTMS.
- Support and coordinate CTMS activities throughout the clinical trial lifecycle.
- Monitor trial-related activities, documentation, timelines, and data updates.
- Coordinate with internal stakeholders and global client teams.
- Ensure proper maintenance, tracking, and reporting of clinical trial information.
- Support resolution of CTMS-related data or operational issues.
Mandatory Requirements
- Minimum 5+ years of experience working on CTMS.
- Strong hands-on experience with Veeva CTMS / Veeva Vault CTMS.
- In-depth knowledge of managing clinical trial data in Veeva.
- Strong understanding of clinical trial processes and CTMS activities.
- Experience managing and controlling CTMS activities across clinical trials.
- Experience working with US and/or European clients.
- Excellent verbal and written communication skills.
- Willingness to work in a US shift.
- Candidates from Delhi NCR are preferred.
- Expected CTC should be within ₹10 LPA.
📌 print (Delhi)
🏢 Assessment360.ai
📍 Delhi
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