purpose of the job:
responsible for adverse event reporting and management of drug safety and pharmacovigilance activities in compliance
responsible for adverse event reporting and management of drug safety and pharmacovigilance activities in compliance
and OOS) documentation and investigations. Adverse Drug Reaction (ADR) support. Root Cause Analysis (RCA)
and OOS) documentation and investigations. Adverse Drug Reaction (ADR) support. Root Cause Analysis (RCA)
requirements, and identify potential risks. Knowledge of drug development, regulations and guidelines Strong leadership
requirements, and identify potential risks. Knowledge of drug development, regulations and guidelines Strong leadership