Drug safety Associate with around 1 years 5 months of experience with adequate exposure in project management activity in Pharmacovigilance
Key assignments:
• Management of case processing activities with extremely high reliability, high quality and in tight timelines according to standard processes and operating procedures.
• Data Entry of serious and non-serious and Quality check of safety data in pharmacovigilance database (ARISg) for purpose of expedited/ periodic reporting and writing adverse event narratives.
• Ensuring timely reporting to various regulatory authorities for expedited cases.
• Review literature articles.
• Create error-free reports and other outputs acco...