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Astha Kothari

@asthakothari

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Pharmacovigilance Technical Associate at IPC who assessed adverse event reports and processed ICSR and PSUR cases.

India

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What I'm looking for

I’m seeking a challenging and responsible position in a professionally managed organization where I can apply my capabilities, skills, and dedication to contribute to the organization’s progress.

At Indian Pharmacopoeia Commission (IPC), I worked as a Pharmacovigilance Technical Associate posted at NATIONAL INSTITUTE OF TUBERCULOSIS AND RESPIRATORY DISEASE. I captured and assessed adverse event reports associated with drug products prescribed by doctors in the hospital.

I processed ICSR and PSUR reports collected from the site, wrote case narratives, and reviewed serious adverse effects reports and forms. I also flagged early warning signs of drug adverse effects and helped minimize the risk of serious side effects.

Earlier, I worked as a Validation associate at JSS Medical research India pvt ltd. and as a Patent analytics Trainee at AnovIP, IPR law firm. My experience includes clinical data validation, query management, patent searches, and technology-field trend studies.

Experience

Work history, roles, and key accomplishments

Pharmacovigilance Technical Associate

Indian Pharmacopoeia Commission

Jul 2019 - Jul 2021 (2 years)

Captured and assessed adverse event reports associated with drug products prescribed by doctors in hospital. Processed ICSR and PSUR, wrote case narratives, and reviewed serious adverse effects reports and forms.

Vigiflow Analyst Clinion Trial Master File PHE Edit MedDRA Microsoft Office Excel Microsoft Word PowerPoint Internet Internal Server

Patent Analytics Trainee

AnovIP

Feb 2019 - Jul 2019 (5 months)

Conducted searches on patentability, validity, freedom-to-operate and infringement. Studied technology field trends and delivered competitive intelligence.

Validation Associate

JSS Medical Research India Pvt Ltd

May 2017 - Jun 2018 (1 year 1 month)

Prepared and updated annotation lists, data validation plans, edit check specifications, and database entries as per study requirements. Performed query management activities and filled data in eCRF for database testing.

Data Validation E CRF Query Management Medical Coding Database Testing