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Divyanka Dubey

@divyankadubey

Content writer and curator at Meril Life Sciences, translating clinical safety information into clear, audience-focused content.

India

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What I'm looking for

I'm transitioning from pharmacovigilance and clinical safety documentation into content writing and content curation, with a focus on health, wellness, and lifestyle writing.

At Meril Life Sciences Pvt. Ltd., I supported digital marketing content for medical device products and wrote safety narratives and regulatory documentation for global audiences. I also contributed writing and data support to safety outcomes for the LANDMARK registry, published in The Lancet and The New England Journal of Medicine.

I'm transitioning from pharmacovigilance and clinical safety documentation into content writing and curation. I self-publish writing on health, wellness, and lifestyle, bringing research, fact-checking, and technical-to-clear writing to my work.

Experience

Work history, roles, and key accomplishments

Assistant Manager, Pharmacovigilance

Meril Life Sciences Pvt. Ltd.

Jun 2025 - Mar 2026 (9 months)

Supported digital marketing efforts for medical device products, including content creation for promotional campaigns and social media assets. Authored safety narratives and regulatory documentation for global audiences, and led a team coordinating deliverables across functions.

Content Creation Digital Marketing Medical Writing Regulatory Documentation Team Leadership Project Management Research Communication Skills

Senior Executive / Executive, Pharmacovigilance

Meril Life Sciences Pvt. Ltd.

May 2023 - May 2025 (2 years)

Reviewed and edited case narratives and safety assessments for clarity, accuracy, and compliance, improving case processing efficiency by 15%. Conducted literature reviews and research synthesis to support signal detection and content accuracy.

Pharmacovigilance Case Processing Medical Writing literature review Research Documentation Compliance

Device Safety Associate, Pharmacovigilance

Meril Life Sciences Pvt. Ltd.

Jan 2022 - Dec 2023 (1 year 11 months)

Wrote and classified device safety reports for regulatory submission, ensuring readability and technical accuracy. Contributed to Risk Management Plans, translating technical risk data into structured, actionable content.

Medical Writing Regulatory Submissions Risk Management Technical Writer Pharmacovigilance

Drug Safety Associate

IQVIA

Jan 2021 - Dec 2022 (1 year 11 months)

Processed and documented adverse event cases with a strong focus on data quality and clarity. Supported training documentation and onboarding content for new team members.

Pharmacovigilance Adverse Event Reporting Data Quality Documentation Training