Open to opportunities

Divya Kagita

@divyakagita

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Detail-oriented pharmacovigilance professional with 2.5 years' global ICSR processing and MedDRA expertise.

United Kingdom

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What I'm looking for

I am seeking remote or Belfast-based pharmacovigilance roles in pharma/CROs where I can apply ICSR processing, MedDRA coding, and quality-focused safety operations while growing in regulatory and QA responsibilities.

I am a Pharmacovigilance Services Associate with 2.5 years of hands-on experience in global ICSR case processing, MedDRA coding, narrative writing, and regulatory compliance with EMA, MHRA and ICH standards. I have processed over 1000 ICSRs across spontaneous, literature and clinical sources, maintained high quality standards, supported periodic safety updates, and collaborated with global QA teams to meet performance KPIs.

I hold an M.Pharm and B.Pharm with strong academic records and certifications in pharmacovigilance, GVP modules, and Power BI. Based in Belfast on a dependent visa and available immediately, I am seeking remote or Belfast-based roles within pharma or CRO environments where I can contribute to robust drug safety operations and continuous quality improvement.

Experience

Work history, roles, and key accomplishments

Pharmacovigilance Associate

Accenture Solutions Pvt. Ltd.

Nov 2023 - Jun 2025 (1 year 7 months)

Processed 1,000+ ICSRs across spontaneous, literature, and clinical sources, performed MedDRA coding and narrative writing, and ensured timely E2B reporting compliant with MHRA and EMA standards while maintaining 100% quality on deliverables.

MedDRA Narrative Writing E2B Reporting GVP ICH MHRA EMA Quality Control

Pharmacovigilance Trainee

Hetero Drugs Pvt Ltd.

Jan 2023 - Nov 2023 (10 months)

Supported literature screening, case triaging, QA audits and data verification, and developed training materials on GVP updates to strengthen regulatory compliance and team workflows.

Literature Screening Triage QA GVP省令 Data Verification