Jane Xu
About Jane Xu
Jane Xu is a Clinical Scientist at Bristol Myers Squibb with extensive experience in clinical safety data review and a background in molecular biology and medicine.
Current Position at Bristol Myers Squibb
Jane Xu is currently working at Bristol Myers Squibb as a Clinical Scientist. She is based in Summit, New Jersey, United States. In her role, she leads safety data review in clinical trials, specifically focusing on Oncology and Immuno-Oncology. This involves significant contributions to clinical study-related documents, ensuring the accuracy and integrity of safety data throughout the clinical trial process.
Previous Experience at Eisai US
From 2020 to 2022, Jane Xu worked as a Clinical Safety Data Review Lead at Eisai US in New Jersey. During her tenure, she oversaw the safety data review for various clinical trials. Her responsibilities included the detailed assessment of clinical data to ensure regulatory compliance and patient safety. She played a crucial role in the development and finalization of clinical study documents.
Senior Scientist at Pfizer
Jane Xu has extensive experience gained from her 16-year tenure at Pfizer, where she served as a Senior Scientist from 2004 to 2020 in Pearl River, NY. Her role involved significant work in clinical studies across multiple therapeutic areas, including oncology, neuroscience, metabolic disorder, and infectious diseases. She brought robust scientific expertise to her projects, contributing greatly to Pfizer's clinical research and development efforts.
Clinical and Academic Background
Jane Xu completed her Bachelor of Medicine at Beijing University, which is equivalent to a Doctor of Medicine in the United States. She specialized in hematology during her medical practice in China. Later, she pursued her Master’s degree in Molecular & Cellular Biology from the University of Maryland, enhancing her expertise in the field.
Molecular Biologist at Johnson & Johnson and Merck
Earlier in her career, Jane Xu worked as a Molecular Biologist at Johnson & Johnson from 2002 to 2004 in Raritan, NJ, and at Merck from 2001 to 2002 in Rahway, NJ. These roles allowed her to build foundational skills in molecular biology, adding to her comprehensive background in clinical and scientific research.
Technical Proficiencies
Jane Xu is technically proficient in Microsoft Office, clinical databases, and clinical data review tools. Her technical skills support her ability to manage and analyze clinical data efficiently, ensuring accurate and thorough safety data review in clinical trials.