Role: Clinical Data Management Coordinator

Experience: 6+ Years

Location: Pan India Remote

Role Overview

We are looking for an experienced Clinical Data Management Coordinator with strong hands-on expertise in Veeva EDC and Veeva CDMS. The candidate will support clinical data management activities, system testing, data quality, and compliance with applicable clinical trial regulations and industry standards.

Key Responsibilities

- Coordinate clinical data management activities across clinical trials.
- Work hands-on with Veeva EDC and Veeva CDMS platforms.
- Support User Acceptance Testing (UAT), including test case preparation, execution, defect tracking, and validation.
- Ensure clinical data accuracy, consistency, completeness, and quality.
- Collaborate with clinical operations, data management,



and cross-functional teams to resolve data-related issues.
- Follow clinical data management best practices and applicable regulatory requirements.
- Support compliance with FDA regulations, ICH guidelines, and relevant industry standards.
- Maintain appropriate documentation for testing, data management processes, and system validation activities.

Mandatory Skills

- 5+ years of relevant experience in Clinical Data Management.
- Strong hands-on experience with Veeva EDC.
- Robust hands-on experience with Veeva CDMS.
- Experience with UAT tools and testing activities.

📌 Clinical Data Management Co-ordinator (India)
🏢 Siro Clinpharm
📍 India