- Review of the world wide scientific and medical literature in accordance with companies-controlled documents.
- Maintain organized records of all literature safety reports received and reported.
- Basic entry of MLM cases received from the authority by uploading and importing XML and RTF files and by analysing received source document.
- Perform duplicate check.
- Manage tracking of MLM cases with source of receipt.
- Ensuring compliance with local regulations and company’s global pharmacovigilance requirement.
- Weekly reconciliation of MLM cases with source of receipt.
- Deliver training to recent joined and team as per requirement.
- Case processing including data entry, drug coding, MedDRA coding, assessment for expediting of ICSR in accordance with company’s standard operating procedure relevant regulations and guidelines.
- Escalate issues or task outside the normal scope of work etc.