Jayesh Jadhav Email & Phone Number | Pharmacovigilance Professional with around 10 years of combined experience in medical coding and pharmacovigilance in Individual Case Safety Report (ICSR) case processing, aggregate report writing including Periodic Safety Update Reports (PSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs), Periodic Adverse Drug Experiences Reports (PADERs), Canadian Annual Reports (CARs), addendum to Clinical Overviews (aCOs), Signal Management Report, Risk Management Plan (RMP). Strong knowledge of Global Pharmacovigilance regulations, ICH-GCP guidelines, and FDA/EMEA/MHRA/MHLW/Health Canada regulations regarding safety of Drugs, Biologics and Medical Devices Quality oriented, with attention to detail. Excellent team player with ability to work independently and to collaborate Manage, plan and organize work assignments and work under strict timelines Excellent written and verbal communication skills Proven interpersonal, analytical thinking, organizational and time management skills

Jayesh Jadhav

Pharmacovigilance Professional with around 10 years of combined experience in medical coding and pha...
Pune, Maharashtra, India

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Jayesh Jadhav’s Location Pune, Maharashtra, India

Jayesh Jadhav’s Current Industry Novartis

Jayesh Jadhav’s Prior Industry Glenmark Pharmaceuticals | Cognizant | Sciformix | Cognizant Technology Solutions

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Medical Safety Writer

2023-07-01 00:00:00 - Present

Assistant Manager

2022-06-01 00:00:00 - 2023-07-01 00:00:00

Team Lead

2020-06-01 00:00:00 - 2022-05-01 00:00:00

Senior Medical Writer

2019-04-01 00:00:00 - 2020-06-01 00:00:00

Junior Data Analyst (Drug Safety Associate)

2014-06-01 00:00:00 - 2015-10-01 00:00:00

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Jayesh Jadhav is a Pharmacovigilance Professional with around 10 years of combined experience in medical coding and pharmacovigilance in Individual Case Safety Report (ICSR) case processing, aggregate report writing including Periodic Safety Update Reports (PSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs), Periodic Adverse Drug Experiences Reports (PADERs), Canadian Annual Reports (CARs), addendum to Clinical Overviews (aCOs), Signal Management Report, Risk Management Plan (RMP). Strong knowledge of Global Pharmacovigilance regulations, ICH-GCP guidelines, and FDA/EMEA/MHRA/MHLW/Health Canada regulations regarding safety of Drugs, Biologics and Medical Devices Quality oriented, with attention to detail. Excellent team player with ability to work independently and to collaborate Manage, plan and organize work assignments and work under strict timelines Excellent written and verbal communication skills Proven interpersonal, analytical thinking, organizational and time management skills