Job Description: -
• Should have knowledge about Adverse Events (AE), PV and Quality check.
• Adverse Event reporting and its source data collection and Verification
• Adverse Event reconciliation
• Listening of sample calls and verifying with respect to AE reporting.
• Review of sample calls of FC, PTC – Interaction summary with respect to AE reporting.
• Sample Audit of Rx with respect to AE reporting.
• Preparing report basics all Audit parameters and sharing with HCAH Management & Client
• Custodian of Adverse Event SOP and Tracker
• Conducting Process training and Pharmacovigilance / Adverse Event Reporting
• Should be responsible for checking all AE’s, AE tracker, Zelthy hygiene check and Coordination with PV team.
• Should be responsible for doing Call quality, Documents check and PV check.
Experience
3 - 6 Years
No. of Openings
1
Education
Graduate (B.Pharma)
Role
Quality Lead
Gender
Female
Job Country
India
Type of Job
Full Time
Work Location Type
Work from Office