David Nichols
About David Nichols
David Nichols is a Senior Clinical Site Monitor at Bristol-Myers Squibb in New Jersey, United States, with extensive experience in clinical research and site management.
Title
David Nichols holds the position of Senior Clinical Site Monitor at Bristol-Myers Squibb in New Jersey, United States. His role involves overseeing various clinical trial processes, ensuring adherence to regulations, and maintaining the safety and protection of study subjects.
Current Company
David Nichols is currently employed at Bristol-Myers Squibb. As part of his responsibilities, he specializes in the Risk-Based Monitoring (RBM) process for clinical trials, ensuring compliance with FDA regulations and Standard Operating Procedures (SOPs). He also manages study site activities through regular on-site visits and telephone communications.
Previous Experience at Novartis
From 2005 to 2012, David Nichols worked at Novartis as a Clinical Research Associate in Basel, Basel-City, Switzerland. During this seven-year period, he was involved in various clinical research activities, contributing to the company's research and development efforts.
Previous Experience at Covance
Before his tenure at Novartis, David Nichols was a Clinical Research Associate at Covance in Princeton, New Jersey. He worked at Covance for five years, from 2000 to 2005, where he gained significant experience in clinical research and trial monitoring.
Education and Expertise
David Nichols studied Biology at Wake Forest University, where he earned a Bachelor of Science degree from 1994 to 1998. His comprehensive background in biology has equipped him with the foundational knowledge necessary for his roles in clinical research and site monitoring.