Associate Data Architect — Clinical Systems & Automation

MSD; Województwo mazowieckie; Hybride; PLN 180 000 - 280 000; Plein temps

Résumé du poste

Merck & Co., Inc. is seeking an Associate Specialist, Data Architect for GDMS Data Integration and Automation.

The role focuses on building, integrating, and maintaining clinical databases and study systems, with responsibilities spanning data logic, tooling, and dashboards. You will collaborate with cross-functional teams to confirm requirements, support UAT, and ensure audit-ready documentation while adhering to GCP and SOP guidelines.

Qualifications

• 2+ years in clinical data programming, data engineering, or related data-management activities.
• Experience with clinical data systems and data validation practices.
• Familiarity with SDLC, SOPs, and audit readiness.

Responsabilités

• Assist design, build, test, and maintain clinical technology systems (EDC/RTSM/eCOA).
• Implement data logic with scripting and validation frameworks.
• Develop and validate tools to streamline design, build, and validation.
• Create dashboards, listings, and visualizations for reporting.
• Configure, test, and validate data sources for integrations.
• Troubleshoot data ingestion issues and support releases under change control.
• Develop data models, queries, and optimize data extracts for reporting.
• Validate functionality and ensure SOP/regulatory compliance with proper documentation.

Connaissances

Python

SQL

SAS

R

Formation

Bachelor’s degree in life sciences / CS / bioinformatics

Associate degree

Advanced degree (MS/PhD)

Outils

EDC

RTSM

eCOA/ePRO

Description du poste

Merck & Co., Inc. is seeking an Associate Specialist, Data Architect for GDMS Data Integration and Automation.

The role focuses on building, integrating, and maintaining clinical databases and study systems, with responsibilities spanning data logic, tooling, and dashboards. You will collaborate with cross-functional teams to confirm requirements, support UAT, and ensure audit-ready documentation while adhering to GCP and SOP guidelines.