Job Description To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding, assessment of seriousness, expectedness, and Company causality, as well as writing of Company comment, follow-up questions and Analysis of Similar Events. This includes completion of all required supporting documentation such as trackers. To support the Qualified Person for Pharm…
Szczegóły oferty
Firma
PrimeVigilance
Lokalizacja
Polska
Kategoria
Unknown
Data publikacji
03.07.2025
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