Anjaly Jayachandran Email & Phone Number | Hi there!! I am a seasoned pharmacovigilance professional with six years of industry experience. My areas of expertise are case processing activities including case receipt, case triage, handling of seriousness check activity, processing adverse events, quality check and medical review (End to End experience in Pharmacovgilance). Processing of adverse events using Argus (includes receipt, assessment of listedness and causality, seriousness criteria / labeling, case prioritization and request follow-ups) based on regulatory requirements. I have strong knowledge in handling affiliate activities including case processing in LAM and performing follow up procedures with consumers and health care professionals. I am trained on narrative writing, PSUR writing and and CIOMS forms for domestic and international cases. I have reviewed, processed, coded, and submitted serious and non-serious adverse event reports for spontaneous and sponsored studies, in compliance with global regulations and compliance timelines. As a senior drug safety associate I have trained and mentored new drug safety associates, providing supervision and teaching key skills.

Anjaly Jayachandran

Hi there!! I am a seasoned pharmacovigilance professional with six years of industry experience. My...
Bengaluru, Karnataka, India

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Anjaly Jayachandran’s Email anjaly.jayachandran@tcs.com

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Anjaly Jayachandran’s Location Bengaluru, Karnataka, India

Anjaly Jayachandran’s Current Industry Tata Consultancy Services

Anjaly Jayachandran’s Prior Industry Accenture | Dental Practice

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Business Process Lead

2022-05-01 00:00:00 - Present

Case Processor

2019-11-01 00:00:00 - 2022-04-01 00:00:00

Dental Surgeon

2017-12-01 00:00:00 - 2018-02-01 00:00:00

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Anjaly Jayachandran is a Hi there!! I am a seasoned pharmacovigilance professional with six years of industry experience. My areas of expertise are case processing activities including case receipt, case triage, handling of seriousness check activity, processing adverse events, quality check and medical review (End to End experience in Pharmacovgilance). Processing of adverse events using Argus (includes receipt, assessment of listedness and causality, seriousness criteria / labeling, case prioritization and request follow-ups) based on regulatory requirements. I have strong knowledge in handling affiliate activities including case processing in LAM and performing follow up procedures with consumers and health care professionals. I am trained on narrative writing, PSUR writing and and CIOMS forms for domestic and international cases. I have reviewed, processed, coded, and submitted serious and non-serious adverse event reports for spontaneous and sponsored studies, in compliance with global regulations and compliance timelines. As a senior drug safety associate I have trained and mentored new drug safety associates, providing supervision and teaching key skills.