Clinical Trial Regulatory Affairs Officer
Ruchi Tiwari
Scientific Writing
Outside Of The Usa, India
6.9 Years
Joined Mar 2026
Iqvia
Clinical Trial Regulatory Management
0 Consultations
About me
Highly motivated Regulatory Affairs and Global Submission professional with 6.8+ years of international experience, including exposure to Germany-based regulatory operations, specializing in global submission strategy, dossier compilation, eCTD publishing, and lifecycle management. Proven track record in supporting complex submissions across major markets while collaborating with cross-functional global teams to ensure regulatory compliance, quality, and timely approvals.
Interests: Microbiology
My Services
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