Pfizer in Buenos Aires, Argentina, is seeking a Senior Associate, Central Monitor, Data Surveillance to ensure data quality and integrity in the clinical trial database under RBM mode. The role involves setting up RBM systems, defining KRIs, and coordinating with the global study team.

Minimum 3–5 years in clinical development and strong data management skills are required. The position follows a hybrid model with 2–3 days in the Pfizer office.