Latam Patient Safety Head

In this role, you will be responsible for monitors and audits the company's drug, biologics or medical devices surveillance program including the intake, evaluation, processing and follow-up on adverse reports. Participates in the resolution of any legal liability and in complying with government regulations. Ensures accurate receipt, maintenance and assessment against product labeling. Reports events or reactions as required by regulatory agencies including adverse events data from clinical trials, spontaneous or solicited sources, periodic and experience reports. May provide trending and safety signal detection and assessment. Supports all clinical trial activity and post marketing.**Commitment to Diversity & Inclusion**:- We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve._**Minimum requirements**- Experience leading patiet safaty areas in pharma companies**Division**SANDOZ**Business Unit**COMMERCIAL OPS EUROPE SZ**Country**Chile**Work Location**Región Metropolitana**Company/Legal Entity**Novartis Chile S.A**Functional Area**Research & Development**Job Type**Full Time**Employment Type**Regular**Shift Work**No**Early Talent**No