Ehsanullah Wedee
About Ehsanullah Wedee
Ehsanullah Wedee is a TMF Study Lead at Bristol Myers Squibb in Princeton, New Jersey, with a background in chemistry and extensive experience in clinical document management.
Current Professional Role
Ehsanullah Wedee is currently employed as a TMF Study Lead at Bristol Myers Squibb. He began this role in October 2020 and operates out of the company's Princeton, New Jersey office. Bristol Myers Squibb is a global pharmaceutical company, and Ehsanullah’s responsibilities likely encompass managing trial master files (TMF), ensuring compliance, and overseeing clinical study documentation processes.
Previous Work Experience
Ehsanullah Wedee has accumulated a diverse range of professional experiences in various roles and companies. Prior to his current position, he worked at Shionogi Inc. as a Records Manager from 2019 to 2020 in Florham Park, NJ. He also held multiple roles at TransPerfect, including Senior Technical Operations Specialist (2017-2019) and Senior Clinical Document Specialist (CDS III) (2017-2018) in New York, NY, as well as a Clinical Document Specialist in Philadelphia, PA (2016-2017). Additionally, Ehsanullah worked as a Chemist at Airgas in Riverton, NJ, for six months in 2016 and as a Document Specialist at Premier Research from 2013 to 2014.
Educational Background
Ehsanullah Wedee pursued his higher education at Temple University, where he studied Chemistry. He obtained a Bachelor of Science (B.S.) degree over the course of five years, completing his studies in 2016. His academic background in chemistry provides a solid foundation for his technical roles in clinical and pharmaceutical settings.
Technical Expertise in eTMF Systems
Ehsanullah Wedee has a strong technical understanding of electronic Trial Master File (eTMF) systems. His expertise spans both the front-end user experience and administrative aspects. Additionally, he possesses a comprehensive knowledge of the TMF Reference Model, ranging from version 2.0 to 3.2. This technical proficiency is essential for his role in managing clinical study documentation and ensuring compliance with regulatory standards.