Job Description

Analyst activities

  • Functional experience and expertise in Pharmacovigilance
  • Develop, maintain, and optimize data workflows within LSMV and LSLI systems.
  • Design and manage SQL queries, stored procedures, and database models to support analytics and reporting needs.
  • Collaborate with business, IT, and QA stakeholders to ensure data quality, integrity, and regulatory compliance.
  • Support integration between LSMV, LSLI, and related platforms to enhance system performance and reporting.
  • Analyze large-scale datasets to identify trends, anomalies, and improvement opportunities.

Testing activities

  • Testing of scenarios in LSMV and LSLI based on the functionalities in all the environments.
  • Using SQL to confirm that all cases, codes, and configurations migrated correctly and that key workflows still function (UAT plus backend validation).
  • New reports or dashboards: validating that front-end metrics (e.g., on-time expedited reporting, open cases, follow-up rates) match SQL-driven counts in the database.




Other Competencies

  • Strong technical expertise, analytical thinking, and the ability to translate complex data workflows into actionable insights for business and regulatory decision-making.
  • Create and maintain technical documentation for SQL processes, data pipelines, and system interactions.
  • Perform data validation and reconciliation across multiple systems or modules.
  • Provide support during audits and inspections by supplying accurate data exports and process evidence.
  • Excellent problem-solving and communication skills with attention to detail.
  • Experience with Argus, Oracle, or PV data systems.
  • Knowledge of ETL tools and data warehouse concepts.
  • Understanding of regulatory data compliance (e.g., GxP, 21 CFR Part 11).
  • Strong expertise in SQL (queries, joins, optimization, troubleshooting).
  • Experience working in pharmaceutical, life sciences, or regulatory data environments preferred.

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