Pharmacovigilance associate
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Dear Hiring Manager,
I am a careful and diligent worker with a strong technical background and relevant experience in pharmacovigilance gained at Novartis.
I relocated recently to the Uk and I am looking forward to resume my career.
First i was hired as POP resource, my taks were:
The management, Collection, processing and archiving of initial and follow up cases of adverse events for all Novartis products (using Argus database)
The submission of safety reports (ICSR) to health authorities within the deadlines imposed by the regulations
Is was also ensuring reconciliations with POP vendor and responsible of the training of the POP vendors
Since March 2020 I became:
Case Processing Lead, my tasks were:
Management of case processing team is Tunisia Morocco and Algeria and working with other local/global Patient Safety associates to ensure accurate evaluation of safety data, monitor national pharmacovigilance regulations and provide update to global Patient Safety department,
Developing and updating local procedures to ensure compliance with Patient Safety global procedures and national requirements,
Ensuring support for and close-out of audits, corrective action plan, investigation
Preparing the submission of KPI reports on compliance in a timely manner including identification of root cause(s) for late reporting to HA, development and implementation of corrective action(s) as needed.
Managing efficient Patient Safety GxP site archive
I was Managing DEA programs trainings and monitoring (SDV)
Performing reconciliation with other departments (e.g., Medical Information, Quality Assurance and third-party contractor) for potential AEs resulting from medical inquiries, quality related complaints and other sources.
I was also Literature screening process lead (Ensuring annual journal selection and monitoring literature screening process and procedures)
