IPV Case Management Specialist Review
at Johnson & Johnson
Placement (10 Months+)
Pharmaceutical
High Wycombe
Review Submitted: August 2024
Overall Rating
4.9 /5
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Overview of Role
Please give an overview of your role and what this involves on a day-to-day basis.
1. Ensuring all Individual Case Safety Reports (ICSRs) containing Adverse Events (AEs) were sent to Drug Safety in a timely manner
2. Compliancing all cases received for Product Quality Complaints (PQCs) and for the correct timelines utilising the Important Medical Events List (IME)
3. Case intake, receipt and triage (IRT) through our safety platform as well as performing preliminary submissions and submissions directly to the Health Authorities
4. Completing Deviation Memos as Corrective Action and Preventative Action (CAPA) for any late case or assisting with Quality Investigations (QI) for multiple late cases
5. Assisting in finding and retrieving information for audits and inspections
6. Taking part in a global workshop and in projects aiming for automation reducing manual repetitive tasks through algorithm-based Artificial Intelligence tools
7. Performing monthly literature reviews and reconciliations for multiple country clusters and liaising with international colleagues