Specialist, Regulatory Data Stewardship (xevmpd / Idmp)

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

Telangana, India
Hybrid
Xevmpd reporting
Idmp data activities
Evweb and veeva vault rim
Be part of an organisation driven by digital technology and data-backed approaches that support a diversified portfolio of prescription medicines, vaccines, and animal health products

Job Summary

  • Be part of an organisation driven by digital technology and data-backed approaches that support a diversified portfolio of prescription medicines, vaccines, and animal health products.
  • As a Regulatory Data Stewards, you will play a pivotal role ensuring the quality of our regulatory data within regulatory domains, which will directly influence patients who use our life-saving products.
  • Our Technology Centers focus on creating a space where teams can come together to deliver business solutions that save and improve lives.

Matching Summary

Be part of an organisation driven by digital technology and data-backed approaches that support a diversified portfolio of prescription medicines, vaccines, and animal health products.

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 regulatory data
  • digital technology and data-backed approaches
  • intellectually curious
  • empathy, creativity, digital mastery

Key Requirements

  • Bachelor’s degree in scientific or IT discipline
  • Minimum 4 years experience
  • Industry regulatory standards and initiatives
  • SmPC / Module 3 knowledge
  • Experience in cross-functional project teams

Work Rights

Not specified

Tailored Resume

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