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manjiri_1234

Manjiri T

@manjiri_1234

Pharmacovigilance Professional Regulatory Affairs Associate

India
English, Marathi, Hindi
About me
I am a results-oriented Pharmacovigilance professional with over 5.5 years of experience in case processing, Argus Safety, and MedDRA coding. I am currently transitioning into Regulatory Affairs with strong knowledge of ICH, GCP, and global health authority expectations. I am recognized for my accuracy, quality, and commitment to regulatory compliance.... Read more

Skills

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manjiri_1234
Manjiri T
Offline • 
Average response time: 1 hour

See my services

Business
I will provide pharmacovigilance case processing and medical review support
From$5 / projectMore details

Work experience

Tata_Consultancy Services

Drug/Patient Safety Specialist

Tata Consultancy Services • Full-time

Mar 2016 - Aug 2021 • 5 yrs 5 mos

Processed Serious Adverse Events (SAE) and non-serious reports using Argus Safety. Performed MedDRA and WHO-DD coding, evaluated causality and seriousness, and drafted clinical narratives. Conducted medical record extraction and assisted in training new associates while ensuring strict regulatory compliance and meeting quality benchmarks.