Merck seeks a Clinical Data Management Associate Specialist to execute core data management activities for clinical trials in Buenos Aires. The role manages data entry, validation, reconciliation, query resolution, and documentation to ensure data quality and regulatory compliance under senior staff direction.
Responsibilities
Execute clinical data management activities for assigned studies per protocols, SOPs, and ICH-GCP requirements
Support data review, reconciliation, logical consistency checks, and remediation across multiple data sources and systems
Manage query workflows and collaborate with sites and service providers to resolve data discrepancies
Identify and escalate data quality issues and risks with supporting context to assigned leadership
Contribute to study documentation including Data Management Plans, Data Validation Plans, and electronic case report forms




Requirements
Minimum 2 years experience in data management, clinical trial operations, or related field
Associate's degree preferred (Nursing, Pharmacy, Life Sciences, Allied Health, or IT); Bachelor's or advanced degree acceptable
Basic knowledge of data collection, analysis, and summarization in research or medical settings
Basic understanding of relational database concepts and data types
Strong attention to detail and ability to follow procedures and compliance requirements
Clear communication skills and ability to document concise notes and status updates
Proficiency in clinical data management, data entry, data validation, and audit trail documentation

📌 Clinical Data Management Associate Specialist (Buenos Aires)
🏢 Merck
📍 Buenos Aires