Assessment of source documents for validity and seriousness.
Case registration and triage in safety database.
Entry of serious and non-serious adverse events into safety database according to work instruction manual, SOPs and relevant data entry instructions.
Extraction of relevant information from documents from various sources (consumer, HCPs, Attorney, license partner etc.) and entry of that information into safety database.
Accurate and timely AE/SAE data entry of cases in safety database and timely processing of follow up cases considering the system-generated due dates for completion.
MedDRA and WHO-DD coding
Job Function- BUSINESS PROCESS SERVICES Role-Analyst Desired Skills-LS – Pharmacovigilance
Desired Candidate Profile
Qualifications :BACHELOR OF PHARMACY, MASTER OF PHARMACY
