Clinical Research Payments Specialist

Veeva CTMS Specialist

Experience: 5+ Years

Work Mode: 100% WFH

Working Days: 5 Days

Shift: US Shift

Preferred Location: Delhi NCR

Client Exposure: US / European clients

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.
• Strong 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.