Specialist, Regulatory Data Stewardship (xevmpd / Idmp)

Merck & Co., Inc., Rahway, New Jersey, USA

Hyderabad, India
Hybrid
Xevmpd reporting
Idmp data activities
Evweb and veeva vault rim
Be part of a global healthcare biopharma company with a 130-year legacy, driven by digital technology and data-backed approaches

Job Summary

  • Be part of a global healthcare biopharma company with a 130-year legacy, driven by digital technology and data-backed approaches.
  • Ensure the quality of regulatory data for XEVMPD reporting to the EMA and for IDMP-related data activities, directly influencing patients.
  • Contribute to data catalogue, data marketplace, and data quality projects to ensure accurate, compliant regulatory data for reporting and business decision-making.

Matching Summary

Be part of a global healthcare biopharma company with a 130-year legacy, driven by digital technology and data-backed approaches.

Skills & Requirements

Must-have

  • XEVMPD reporting
  • IDMP data activities
  • EVWEB and Veeva Vault RIM
  • European regulatory framework
  • data migration and enrichment

Nice-to-have

  • passion for data management
  • digital technology driven
  • data-backed approaches
  • intellectually curious
  • empathy and creativity

Key Requirements

  • Minimum 4 years experience
  • Bachelor's degree in scientific or IT discipline
  • Strong working knowledge of XEVMPD/EVPRM
  • Good understanding of SmPC and Module 3
  • Experience in cross-functional project teams

Work Rights

Not specified

Tailored Resume

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