Senior Associate, Central Monitor, Data Surveillance, Clinical Data Sciences

Work Location: Buenos Aires, Argentina (Complejo LUMINA – Office Park). This role follows a hybrid model; colleagues are expected to work from the assigned Pfizer office 2–3 days per week, or as required by business needs.

Our mission is straightforward: support healthcare decisions that ensure the safe and effective use of medications. By ensuring our evidence is sound and offering necessary medical insights, we strive to improve patient care and treatment efficacy.

The Senior Associate, Central Monitor is responsible for ensuring the completeness, quality and integrity of the subject data in the clinical trial database under Risk‑Based Monitoring (RBM) mode. The core areas of activity include:

• Develop a Risk‑Based Monitoring system for applicable studies.
• Ensure key risk indicators (KRIs) are properly defined and set up in the system to support the study.
• Process and review study data in the system for signal and action management.