Study Start-Up Clinical Research Associate

**Summary**:- Monitors patient data and study-related information related to clinical study sites and clinical trial participation.Ensures the investigator adheres to research protocols, regulatory requirements and good clinical practices and provides input into data validation plan.Provides timely and accurate monitoring of patient data & study-related information from source documents, research records, and site visits where applicable.May monitor study sites and audit facility selection.
**About the Role**:**Major accountabilities**:- Assist the clinical research team in preparing safety reports document for Investiga -Normally receives detailed instructions on all work -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)**Key performance indicators**:- Deliver customer satisfaction results for internal and external customers -Delivery of Clini...