Medical Data Reviewer (MDR)

Responsibilities :

• Review subject/ patient level data for accuracy, to identify any anomalies, trends in patient reported data
• Review and provide inputs ion design of eCRF
• Review investigation product dosing
• Review all reported Adverse Events (AEs) , Concomitant Medication and medical
• Ensure that any ‘out of range’ data/ anomaly is verified
• Review all laboratory data of study subjects
• Review data in the form of visualizations and identify potential issues of concern
• Training of new team members

• Good English communication skills
• Experience of handling clinical trial/ safety data - > 4 years