Consultant - Pharmacovigilance Rédaction PSUR H/F
Ividata Life Sciences
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Full Time
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4 months ago
Ividata Life Sciences
The consultant will pilot and write PSUR/PBRER documents in compliance with ICH E2C(R2) and GVP Module VII, coordinating cross-functional contributors to ensure scientific coherence with CCDS, RSI, and RMP documents.
