Melanie Benito
About Melanie Benito
Melanie Benito is the Associate Director, Risk Management Lead, Clinical Compliance at Bristol-Myers Squibb with over two decades of experience in the pharmaceutical industry, specializing in clinical trials and compliance.
Current Position at Bristol-Myers Squibb
Melanie Benito is currently serving as the Associate Director, Risk Management Lead, Clinical Compliance for Global Clinical Operations at Bristol-Myers Squibb. Based in New Jersey, United States, she plays a pivotal role in overseeing risk management and ensuring clinical compliance in global clinical operations. Her responsibilities likely encompass the identification and mitigation of risks associated with clinical trials, ensuring adherence to regulatory standards, and maintaining high levels of clinical compliance.
Previous Roles at Bristol-Myers Squibb
Melanie Benito has an extensive history with Bristol-Myers Squibb, having worked in various capacities over two decades. She was a Senior Clinical Scientist 2 in Oncology Clinical Protocol Operations from 2016 to 2018 and a Senior Clinical Scientist 1 in Early Clinical and Translational Research from 2014 to 2016. Prior to these roles, she served as a Clinical Scientist in Discovery Medicine and Clinical Pharmacology from 2010 to 2014, and as an Associate Clinical Scientist in the same department from 2007 to 2010. She also worked as a Quality Compliance Associate in Global Quality and Regulatory Compliance from 2005 to 2007 and started her journey at Bristol-Myers Squibb as an Associate Clinical Supply Scientist in Clinical Supply Operations from 2001 to 2005.
Educational Background
Melanie Benito earned her Master of Science degree from Temple University, where she studied from 2005 to 2008. Before that, she completed her Bachelor of Science in Chemistry at Adamson University. Her robust educational background laid a foundation for her comprehensive understanding of clinical practices and pharmaceutical sciences, which she applies in her professional role.
Experience in Clinical Trials and Therapeutic Areas
Melanie Benito has extensive experience managing clinical trials across a range of therapeutic areas, including Oncology, Immunology, Metabolic, and Neuroscience. Her expertise spans the phases of clinical trials from Phase 1 to Phase 3. This comprehensive understanding of various therapeutic areas and trial phases underpins her current role in risk management and clinical compliance.
Skills in Good Clinical Practice and Clinical Protocol Development
Melanie Benito is skilled in Good Clinical Practice (GCP) and the development of clinical protocols. These skills are critical in her role as Associate Director, ensuring that all clinical operations adhere to the highest standards of ethical and scientific quality. Her experience in clinical compliance and risk management further enhances her ability to oversee and direct clinical trials effectively.