I am a Pharm. D graduate with PGDPRA. I have almost 1.3 years of experience in RA. During this tenure I got hands on experience in core areas of RA like Dossier compilation(M1 - M5) , Post approval Variations, Query management , stakeholder &customer management & so on. Seeking for opportunities which enables me have hands on experience in Regulatory tools like RIMS, Veeva,. Please help if anyone can refer me in GSK

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