Clinical Data Management Co-ordinator
Siro Clinpharm · Remote · remote · Posted 9d ago
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About this role
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.
- Strong hands-on experience with Veeva CDMS.
- Experience with UAT tools and testing activities.
Sourced from naukri
Skills
About SIRO Clinpharm

Siro Clinpharm
Pharma
329
employees
1996
30 years old
Mumbai
India
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