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 within regulatory domains, directly influencing patients who use life-saving products.
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
regulatory data quality
Nice-to-have
digital technology and data-backed approaches
passion for using data
custom software development
intellectually curious
empathy, creativity, digital mastery
Key Requirements
Bachelor’s degree in scientific or IT discipline
Minimum 4 years experience
Strong working knowledge of industry regulatory standards
Good understanding of European regulatory framework