Pharmacovigilance Associate
Pharmacovigilance Program Of Indi
Total years of experience :9 years, 8 Months
Key responsibilities:
•Responsible for drafting case narratives and processing case-related information.
•To perform initial triage of the received safety notifications as per client protocol.
•To process Individual Case Safety Reports (ICSRs), including data entry in safety database.
•Performing MedDRA coding assessment
Other
•Twenty six months experience
Area of Interest:
•Pharmacovigilance Operations and Clinical Trial.
•Area of Expertise:
•ADR Reporting
•MedDra Coding
•Patient Counseling
in
courses: Certified online course in Causality assessment
courses: Certified course in Pharmacovigilance