Shana Indawala, Pharm D
About Shana Indawala, Pharm D
Shana Indawala, Pharm D, is a Scientist and Scientific Writer I at Bristol Myers Squibb in Summit, New Jersey. She has a diverse background in pharmacy and medical writing, with experience in community, institutional, and geriatrics pharmacy settings.
Title
Shana Indawala holds the title of Scientist, Scientific Writer I at Bristol Myers Squibb in Summit, New Jersey, United States. She has been contributing to the company's development of scientific and regulatory documentation.
Current Employment at Bristol Myers Squibb
Shana Indawala is currently employed at Bristol Myers Squibb as a Scientist, Scientific Writer I based in Summit, New Jersey, United States. In her role, she focuses on developing scientific and regulatory documentation to support the company’s projects.
Previous Experience in Community and Institutional Pharmacy
Shana Indawala has diversified experience in both community and institutional pharmacy settings. She worked as a Community Pharmacy Extern at Suncoast Community Health Centers, Inc., an Institutional Pharmacy Extern at AdventHealth, and a Geriatrics Pharmacy Extern at Reliance Healthcare. These roles have equipped her with a broad understanding of different pharmacy practices.
Education and Expertise
Shana Indawala earned her Doctor of Pharmacy (PharmD) degree with a concentration in Health Education from the University of South Florida Health Taneja College of Pharmacy, where she studied from 2017 to 2021. She also holds a Bachelor of Science degree in Biomedical Sciences with a minor in Nutrition from the University of South Florida, which she completed in 2017. Her academic background has given her a solid foundation in both pharmacy and biomedical sciences.
Experience as a Medical Writer
Shana Indawala gained extensive experience in medical writing, particularly in diabetes management, during her externship at Diabetes In Control in Tampa, Florida. She also interned as a Clinical Writer at CONMED Corporation for two years, focusing on clinical documentation. These roles provided her with substantial experience in crafting scientifically accurate and regulatory-compliant medical documentation.