0 - 2 years
0 Lacs
Posted:17 hours ago|
Platform:
On-site
Full Time
Collect and document adverse event information from healthcare professionals, patients, and literature.
Enter case details accurately into the safety database.
Assist in the initial assessment of seriousness and expectedness of reported events.
Maintain and update pharmacovigilance databases under supervision.
Support in the retrieval and tracking of safety information.
Assist in preparing and submitting individual case safety reports (ICSRs) to regulatory authorities within defined timelines.
Ensure adherence to company standard operating procedures (SOPs) and Good Pharmacovigilance Practices (GVP).
Support in preparation of safety reports such as PSURs, DSURs, and RMPs.
Maintain accurate and organized case documentation
CLARIWELLGLOBAL SERVICES LLP
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