Found Description
As a Graduate Pharmacovigilance Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
**What you will be doing**:
- Submission of expedited Serious Adverse Event (SAE) reports, Periodic reports, line listings and applicable safety information to clients, Regulatory Authorities, Ethics Committees, investigators, third party vendors, Partners, and ICON personnel, if required & as agreed with client during study set-up, within study specified timelines.
- Develop understanding of ICON's safety reporting systems, processes, and conventions, as appropriate.
- Develop understanding of ICON Standard Operating Procedures (SOPs), Working Procedures (WPs), guidance documents and manuals associated with safety reporting.
- Support filing activities in the eTMF ensuring file readiness on assigned projects for audits or inspections.
- Serve as safety reporting or quality complaint processor for as...
**What you will be doing**:
- Submission of expedited Serious Adverse Event (SAE) reports, Periodic reports, line listings and applicable safety information to clients, Regulatory Authorities, Ethics Committees, investigators, third party vendors, Partners, and ICON personnel, if required & as agreed with client during study set-up, within study specified timelines.
- Develop understanding of ICON's safety reporting systems, processes, and conventions, as appropriate.
- Develop understanding of ICON Standard Operating Procedures (SOPs), Working Procedures (WPs), guidance documents and manuals associated with safety reporting.
- Support filing activities in the eTMF ensuring file readiness on assigned projects for audits or inspections.
- Serve as safety reporting or quality complaint processor for as...