Specialist, Regulatory Data Stewardship (xevmpd / Idmp)
Mericalherbs
Hyderabad, , India
Hybrid
Xevmpd submissions management
Idmp data governance
Evweb and veeva vault rim proficiency
Join a global healthcare biopharma company with a 130-year legacy focused on ethical integrity and innovation in global healthcare
Job Summary
Join a global healthcare biopharma company with a 130-year legacy focused on ethical integrity and innovation in global healthcare.
As a Regulatory Data Steward, you will ensure the quality and regulatory readiness of product registration data impacting life-saving medicines and vaccines.
The role involves managing XEVMPD and IDMP submissions, coordinating compliance activities, and supporting data quality and enrichment initiatives.
Matching Summary
Join a global healthcare biopharma company with a 130-year legacy focused on ethical integrity and innovation in global healthcare.
Skills & Requirements
Must-have
XEVMPD submissions management
IDMP data governance
EVWEB and Veeva Vault RIM proficiency
Regulatory data quality assurance
European Medicines Agency compliance
Data migration and enrichment
Nice-to-have
Power BI familiarity
Cross-functional project experience
Effective communication and collaboration
Autonomous and methodical work style
Experience with Microsoft 365 apps
Adaptability and problem-solving skills
Key Requirements
Bachelor’s degree in scientific or IT discipline
Minimum 4 years regulatory affairs experience
Strong knowledge of XEVMPD, IDMP, SPOR, RIM systems
Understanding of European regulatory framework
Experience with EVWEB and Veeva Vault RIM
Experience in data migration and enrichment projects