Pfizer seeks a Senior Associate, Central Monitor to ensure data quality and integrity in clinical trial databases using risk-based monitoring. The role involves setting up monitoring systems, defining risk indicators, reviewing study data, and coordinating with general teams to support safe and effective medication use.
Responsibilities
Set up, test, and maintain risk-based monitoring systems at study level
Define and validate key risk indicators and data quality assessment dictionaries
Review system outputs to identify signals and coordinate issue resolution
Develop quality control documentation and ensure RBM compliance with protocols and regulations
Facilitate cross-study learning by documenting and sharing lessons learned
Requirements
Bachelor's degree or equivalent in scientific or business discipline
3–5 years clinical development experience
Data management background including CRF design and database setup
Knowledge of clinical trial databases and Windows applications
Experience with Oracle, PL/SQL, SAS, Java, or relational database design
Understanding of Phase I–IV study design and regulatory principles
Project management and stakeholder communication skills

📌 Senior Associate, Central Monitor, Data Surveillance, Clinical Data Sciences (Buenos Aires)
🏢 Pfizer
📍 Buenos Aires