Reema Baweja
About Reema Baweja
Reema Baweja is the Associate Director of Clinical Data Standards at Bristol Myers Squibb, with 14 years of experience in clinical research and data standards.
Title
Reema Baweja is currently serving as the Associate Director, Clinical Data Standards at Bristol Myers Squibb. She has extensive experience in clinical data standards and regulatory compliance.
Current Company
Reema Baweja is employed by Bristol Myers Squibb, where she holds the position of Associate Director, Clinical Data Standards. She is responsible for overseeing the development and implementation of clinical data standards.
Previous Work Experience
Before joining Bristol Myers Squibb, Reema Baweja worked at Celgene for 7 years. She served as the Senior Manager, Clinical Data Standards from 2019 to 2021 in Berkeley Heights, New Jersey, and as Manager- Global Data Standards from 2014 to 2019. Earlier in her career, she worked at Forest Laboratories as a Senior Standards Analyst from 2012 to 2014 in New Jersey. She also gained significant experience at Cognizant Technology Solutions, where she worked as a Subject Matter Expert (SME)- CDISC-SDTM from 2008 to 2012.
Education and Expertise
Reema Baweja holds an M.Sc. in Biotechnology from Bangalore University, achieved between 2005 and 2007, and a B.Sc in Biotechnology from the Institute of Applied Medicine & Research completed in 2005. Additionally, she studied Pharmacovigilance & Pharmacoepidemiology at Symogen India for a year from 2007 to 2008.
Achievements
Reema Baweja has successfully worked on four New Drug Application (NDA) submissions, showcasing her expertise in regulatory requirements and clinical data standards. She also has consulting experience, providing guidance on CDISC models and domains. With 14 years of professional experience in clinical research and clinical data standards, she possesses extensive knowledge of the clinical study process and the creation and validation of CDISC SDTM compliant domains.