Natalie Arotsky
About Natalie Arotsky
Natalie Arotsky is a Senior Central Monitor at Bristol-Myers Squibb in Princeton, NJ, with extensive experience in clinical data management and risk-based monitoring.
Title
Natalie Arotsky holds the position of Senior Central Monitor at Bristol-Myers Squibb. In this role, she is based in Princeton, NJ, and oversees the monitoring of clinical trials, ensuring adherence to regulatory guidelines and effective data management.
Experience at Bristol-Myers Squibb
Natalie Arotsky has extensive experience working at Bristol-Myers Squibb in various roles. She has been serving as a Senior Central Monitor, focusing on risk-based monitoring and quality management. Prior to this, she spent 13 years as a Senior Protocol Data Manager, where she managed phase I-IV clinical trials across multiple therapeutic areas including cardiovascular, oncology, diabetes, and neuroscience. Her expertise includes project management and vendor/CRO oversight.
Previous Roles in Clinical Data Management
Earlier in her career, Natalie Arotsky worked at PharmaNet, Inc. as a Clinical Data Manager. During her tenure from 1999 to 2002, she managed clinical data and ensured compliance with regulatory standards. Before joining PharmaNet, she served as a Clinical Data Analyst/Protocol Leader at Merck & Co., Inc. from 1995 to 1999, where she focused on clinical data analysis and protocol management.
Educational Background
Natalie Arotsky has a diverse educational background. She studied Chemical/Biomedical Engineering and Environmental Science, Chemistry, and Biological Science at Kharkov State Scientific Academy of Municipal Economy, earning a Master's degree. Additionally, she attended Info Source School of Information Technology in Huntington Valley, PA, where she achieved proficiency in various IT and database management tools, including Visual Basic, SQL, MS ACCESS, and more.
Expertise in Data Management and Risk Based Monitoring
Natalie Arotsky is well-versed in data management procedures and industry standards. She excels in the use of electronic data capture systems such as Rave, Inform, and RDC. As part of her role at Bristol-Myers Squibb, she supports the execution of Risk Based Monitoring/TransCelerate processes, contributes to global monitoring, and aids in the development of business processes for risk mitigation. She plays a crucial role in training, global inspection readiness, and partnership relationship support.