Bhoomi Pandya Email & Phone Number | Experienced in field of pharmacovigilance • Write accurate narrative for safety Reports and Medical writing following ICH Guidelines and SOP’s • Sound knowledge of ARGUS and IRMS (client database) and clinical Research operations. • Following client specified SOP’s and meeting deadlines • Receive spontaneous and solicited adverse event reports from Health care professionals and forward the same with client specified time line with identification of case type. • Clinical review of all cases- Serious and Non serious Safety Reports. • Performing validity assessment for all cases and determining the seriousness of the events. • Booking case into Client’s corporate safety database (ARGUS) and attaching Adverse Event Report (Source Document) from the case, routing case appropriately either for primary review, data entry or invalid state. • Coding of suspect product and concomitant product using WHO dictionaries. • Ensuring events in all types of cases are coded appropriately. • Determine and perform appropriate case follow-up, generating and requesting follow-up letters. • Applications used Argus. Types of cases processed: • Spontaneous • Literature • Social Media • Contract Partner • Clinical Trials Apart from all professionals expertise and keen to my interest, I have knowledge of various guidelines like ICH-GCP, schedule Y, EU guidelines and Good pharmacovigilance practice. I am also interested in area of medical writing and other clinical aspects.

Bhoomi Pandya

Experienced in field of pharmacovigilance • Write accurate narrative for safety Reports and Medica...
Bengaluru, Bengaluru, India

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Bhoomi Pandya’s Email bhoomi.pandya@cognizant.com

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Bhoomi Pandya’s Location Bengaluru, Bengaluru, India

Bhoomi Pandya’s Current Industry Iqvia

Bhoomi Pandya’s Prior Industry Cognizant Technology Solutions

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Work Experience

Iqvia

Medical Writer Ii

2022-04-01 00:00:00 - Present

Cognizant Technology Solutions

Junior Saftey Data Anlysist

2012-09-01 00:00:00 - 2013-05-01 00:00:00

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FAQ About Bhoomi Pandya

Bhoomi Pandya is located at
Bengaluru, Bengaluru, India

Bhoomi Pandya is a Experienced in field of pharmacovigilance • Write accurate narrative for safety Reports and Medical writing following ICH Guidelines and SOP’s • Sound knowledge of ARGUS and IRMS (client database) and clinical Research operations. • Following client specified SOP’s and meeting deadlines • Receive spontaneous and solicited adverse event reports from Health care professionals and forward the same with client specified time line with identification of case type. • Clinical review of all cases- Serious and Non serious Safety Reports. • Performing validity assessment for all cases and determining the seriousness of the events. • Booking case into Client’s corporate safety database (ARGUS) and attaching Adverse Event Report (Source Document) from the case, routing case appropriately either for primary review, data entry or invalid state. • Coding of suspect product and concomitant product using WHO dictionaries. • Ensuring events in all types of cases are coded appropriately. • Determine and perform appropriate case follow-up, generating and requesting follow-up letters. • Applications used Argus. Types of cases processed: • Spontaneous • Literature • Social Media • Contract Partner • Clinical Trials Apart from all professionals expertise and keen to my interest, I have knowledge of various guidelines like ICH-GCP, schedule Y, EU guidelines and Good pharmacovigilance practice. I am also interested in area of medical writing and other clinical aspects.