Komal Shah is a highly qualified expert, working in Takeda Pharmaceuticals as a Associate Director, Global Safety Scientist since 2019. Komal gained professional experience in more than six positions at different companies. Komal Shah went to the Northeastern University and received education there from 2015 to 2017. Komal has these qualifications: Six Sigma Yellow Belt, Train the Trainer, and Tata Consultancy Services. Boston, Massachusetts is the area, where this person was known to be living. This expert's phone and email are easily accessed through SoftwareOfficial on demand.
Name variants:
Komal Shah
Last updated May 31, 2024
Contact Information
Last Update
Jun 22, 2022
Email
ko**@baxalta.com, sm**@gmail.com
Location
Boston, MA
Company
Takeda Pharmaceuticals
Workplace
Associate Director, Global Safety Scientist
Work History
Associate Director, Global Safety Scientist
Patient Safety - Aggregate Reports, Signal Management, Risk Management Activities
from Jan 2019
Associate Director, Safety Analytics and Reporting
Drug Safety Surveillance - Aggregate Reports, Signal Management, Risk Management Activities
Jul 2018 — Dec 2018
Analytics and Reporting Lead, Global Drug Safety
Responsible for review and reporting of aggregate safety data from various sources in support of regulatory reporting requirements, activities pertaining to our products. This includes:
Co...
Nov 1, 2016 — Jun 2018
Analytics and Reporting Lead , Global Drug Safety
Illinois
Pharmacovigilance Safety Analytics & Reporting Responsible for aggregate review and reporting of safety data from various sources in support of regulatory aggregate reporting requirements, a...
Feb 2016 — Nov 2016
Medical Writer, Scientific Writing and Regulatory Affairs
206 Carnegie Ctr Dr, Princeton, NJ
Jul 2013 — Jul 2015
Education
2015 — 2017
2005 — 2011
2003 — 2005
1993 — 2003
Occupations
Executive
Deputy Director
Scientist
Deputy Manager
Chief Executive
Skills
Pharmacovigilance
Ich Gcp
Medical Writing
Drug Safety
Meddra
Clinical Trials
Gcp
Regulatory Affairs
Regulatory Submissions
Pharmaceutical Industry
Fda
Clinical Research
Sop
Healthcare
Life Sciences
Good Clinical Practice
Aggregate Reporting
Cfr
Medicine
Safety Reports
Project Management
Data Analysis
Quality Reviews
Capa
Internal Audit
Regulatory Requirements
Time Management
Problem Solving
Six Thinking Hats
Team Leadership
Lean Six Sigma
Scientific Writing
Pader
Pbrer
Canadian Annual Report
Brazilian Periodical Pharmacovigilance Report
Psurs
Dsur
Standard Operating Procedure