Danielle Adams Chell
About Danielle Adams Chell
Danielle Adams Chell is the Associate Director of Global Scientific and Regulatory Documentation and a Senior Scientific Writer at Bristol-Myers Squibb in Princeton, NJ.
Current Role at Bristol-Myers Squibb
Danielle Adams Chell serves as the Associate Director, Global Scientific and Regulatory Documentation, and Senior Scientific Writer at Bristol-Myers Squibb in Princeton, NJ. In her current role, she coordinates and authors various regulatory submissions, such as Phase 1/2 Clinical Study Reports, briefing documents, CTD summary documents, and Investigator Brochures. She ensures the integration of scientific, medical, and regulatory inputs from the development team, manages timelines, and resolves issues to ensure timely and high-quality document completion.
Previous Experience at Bristol-Myers Squibb
Prior to her current role, Danielle Adams Chell worked as a Clinical Protocol Manager at Bristol-Myers Squibb from 2008 to 2013. Before that, she served as a Clinical Scientist at the same company from 2005 to 2008. Both of these positions were also based in Princeton, NJ. During these years, she gained extensive experience in clinical science and protocol management.
Educational Background
Danielle Adams Chell obtained her Bachelor of Science (BS) degree from The College of New Jersey. Her educational background laid the foundation for her extensive career in scientific writing and regulatory documentation within the pharmaceutical industry.
Key Responsibilities and Expertise
In her role, Danielle Adams Chell is tasked with coordinating and authoring documents for regulatory submissions. She participates in document sub teams to ensure the effective planning and management of timelines, coordinates the review process, and resolves issues to maintain high-quality standards. Additionally, she analyzes and interprets clinical data from various therapeutic areas and coordinates the writing of responses to Health Authority questions.