(Sr) Safety Scientist/associate Safety Director
vor 17 Stunden
**You will be Responsible For Activities including**:
Aggregate case reporting (ICSR), aggregate report (DSUR, PSUR), signal detection/management, safety strategy, input to clinical development strategy (from safety perspective), Risk management (CCDS, IB, RMP, IND/NDA, MAA), support, presentations, publications, vendor relations
**You will bring the following**:
Medical Doctor qualification with post qualification clinical/patient facing experience. (Board certification would be a bonus)
+4 years drug development and minimum 2 years drug safety experience in CRO/BioTech/Pharma.
GxP / Regulated process
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