Job Details

The Fountain Group is seeking a pharmacovigilance specialist to handle ICSDR case processing and QC for clinical trials and post-market events. You will perform narrative writing, MedDRA coding, and draft follow-up queries to stakeholders, ensuring timely regulatory submissions from Biogen studies and other assignments.

Ideal candidates bring 4+ years in pharmacovigilance, strong regulatory knowledge (FDA/ICH/EU), and hands-on experience with safety databases such as ArisG, Argus, and Veeva,