Key Responsibilities :

Analyze and document business requirements related to pharmaceutical data, terminology governance, and regulatory information systems.

Collaborate with cross-functional teams including Regulatory Affairs, IT, and Data Governance to drive data integrity and compliance initiatives.

Support implementation and maintenance of master data systems (RIM, MDM) and ensure alignment with global regulatory data standards.

Manage and maintain controlled medical vocabularies including XEVMPD, MedDRA, WHO-DD, SNOMED, IDMP, and SPOR.

Leverage SQL and APIs for data extraction, transformation, and integration tasks across regulatory systems.

Skills and experiences required :

- Bachelor's degree in Life Sciences, Pharmacy, Information Systems, or related field.

- 8-10+ years' experience in pharmaceutical data management, terminology governance, or regulatory systems.

- Strong understanding of controlled medical vocabularies (XEVMPD, MedDRA, WHO-DD, SNOMED, IDMP, SPOR).

- Proficiency with RIM, MDM, or other master data systems

- Proficiency with SQL, familiarity with working on APIs and system integrations is a plus.

- Excellent analytical, documentation, and stakeholder management skills.

- Knowledge of global regulatory submission processes and data standards.