Analyst Pharmacovigilance
Analyst Pharmacovigilance
Analyst Pharmacovigilance
3) Update ADR tracker with new information, write ADR narratives, report ADRs to regulatory authorit
5) Prepare annual safety reviews for products and maintain a good knowledge of current pharmac
SOPs.
6) Develop appropriate understanding of DSS case processing, required DSS and company SOPs, codi
7) Develop expert technical understanding of the relational design and structure of the corporate
variable definitions, as well as similar information in other safety data sets, such as those from clinica
8) Report generation and authoring includes sections that PVRM is responsible for in regulatory repo
regulators, requests from key stakeholders, such as Clinical Research.
9) Assist in developing routine and non-routine PVRM evaluations of safety data by developing repo
sources, including the corporate safety database and safety data from ABPs, and author a pre
methodology and factual summaries of output to assist the medical resources in their evaluation o
reports, events of interest, and evaluation of potential signals.
Experience 3 - 5 Yea
Education UG - B.P
Medicine;
Specializa
PG - Any PG Course - Any Specialization
Location Delhi
Keywords Analyst p
Email hrd@pana
Reference 0225/PAN
(Referen
mention