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Nederlands
$
USD
Manjiri T
@manjiri_1234
Pharmacovigilance Professional Regulatory Affairs Associate
India
Engels, Marathi, Hindi
Over mij
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.
Skills
Manjiri T
offline •
Gemiddelde reactietijd: 1 uur
Bekijk mijn diensten
Zakelijk
I will provide pharmacovigilance case processing and medical review support
Werkervaring
Drug/Patient Safety Specialist
Tata Consultancy Services • Fulltime
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.
