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Larianna Kazmerchuk

@lariannakazmerchuk

Message

I review pharmaceutical dossiers and regulatory evidence for EAEU product compliance.

Uzbekistan

Message

What I'm looking for

I'm looking to contribute my pharmaceutical and regulatory subject-matter knowledge to AI training, evaluation, and medical-content quality initiatives, especially work involving the review of complex medical and regulatory documentation.

I've managed approximately 20 concurrent EAEU pharmaceutical harmonization projects at a Regulatory Affairs Consulting Company, coordinating dossiers, timelines, regulatory deliverables, and outstanding actions.

I prepare and review CTD Modules 1–3, conduct regulatory research, and develop evidence-based responses to Health Authority questions and deficiency letters. My work focuses on finding gaps, inconsistencies, and compliance issues in complex pharmaceutical and scientific documentation.

I've also supported post-approval changes, lifecycle management, GMP inspection documentation, version control, regulatory databases, and submission-readiness reviews.

With a Specialist's Degree in Pharmacy, C1 English, and native Russian and Ukrainian, I'm interested in applying my pharmaceutical subject-matter knowledge to AI training, evaluation, and medical-content quality initiatives.

Experience

Work history, roles, and key accomplishments

Regulatory Affairs Specialist

Regulatory Affairs Consulting Company

Apr 2024 - May 2026 (2 years 1 month)

Managed approximately 20 concurrent EAEU harmonization projects for pharmaceutical products, coordinating regulatory deliverables, documentation, timelines, milestones, and outstanding actions. Prepared, reviewed, maintained, and finalized CTD Modules 1–3 and pharmaceutical regulatory dossiers in accordance with EAEU requirements.