
Safety science coordinator 1 focuses on adverse event monitoring, patient safety documentation, and timely escalation of clinical concerns in regulated care settings. Clinical work in COVID-19 care supports accurate note taking, structured case review, and disciplined reporting under emergency protocols. Multidisciplinary collaboration helps maintain continuity of care while strengthening patient safety reporting and case quality.
Icsr case processing (initial & follow-up)
Adverse event / adr identification
MedDRA & who-dd coding
Causality assessment (WHO-UMC, Naranjo)
Expedited reporting & susar timelines
Literature screening
Case narrative writing
Follow-up query management
Safety data reconciliation
Quality control review
Aggregate safety reporting
Periodic safety update reports
Pharmacovigilance certification