Pfizer · Buenos Aires, Argentina · Hybrid · Argentina
Central monitoring for clinical trials: sets up and tests the risk-based monitoring system per study, defines key risk indicators and data-quality checks, and works issues through with study teams. Bachelor's in a scientific or business field or equivalent experience, and 3 to 5 years in clinical development. Hybrid at the Buenos Aires office; apply with an English CV. No clinical license. Pay not posted. Requisition 4966013.
Biology / biomedical science · Data science / analytics · Business / health administration
risk-based monitoring (RBM) · key risk indicators · data quality assessment · ICH GCP