Clinical Data Validation & Systems Automation Specialist

Merck; Województwo mazowieckie; On-site; PLN 90,000 - 130,000; Full time

Job summary

Merck's Global Data Management & Standards (GDMS) Data Integration and Automation team seeks a Business System Validation Associate Specialist to execute and document validation activities ensuring data quality, system integrity, and regulatory compliance across data pipelines and automation workflows.

You will perform study-specific validation tests, maintain audit-ready documentation, and contribute to validation summary reports, collaborating with cross-functional partners to support clinical

Qualifications

• Non-Degree with minimum 2 years of experience in validation/testing role
• Associate's Degree with minimum 1 year in validation/testing role
• Bachelor's or Advanced Degree with prior relevant field experience (preferred)
• Experience with GxP, CSV and regulatory guidelines is preferred

Responsibilities

• Validation planning, strategy and readiness and data integrity checks across data pipelines and automation workflows
• Test execution, defect management and retesting per established procedures; participate in AI-testing and automation pilots
• Documentation, compliance and continuous improvement; prepare validation summary reports and maintain audit-ready documentation

Skills

Adaptability

Analytical Problem Solving

Data Integrity

Data Validation

Data Privacy

Education

Bachelor's Degree in a relevant field

Associate's Degree

Non-Degree with 2+ years experience

Tools

Test Management Tools

Clinical Data Management Systems

Job description

Merck's Global Data Management & Standards (GDMS) Data Integration and Automation team seeks a Business System Validation Associate Specialist to execute and document validation activities ensuring data quality, system integrity, and regulatory compliance across data pipelines and automation workflows.

You will perform study-specific validation tests, maintain audit-ready documentation, and contribute to validation summary reports, collaborating with cross-functional partners to support clinical