Sandra Pacheco
About Sandra Pacheco
Sandra Pacheco is a Clinical Regulatory Affairs Specialist at Nutrasource in Guelph, Ontario, with over 25 years of experience in the pharmaceutical industry, specializing in Good Clinical Practice and ICH guidelines.
Work at Nutrasource
Sandra Pacheco has been employed at Nutrasource as a Clinical Regulatory Affairs Specialist since 2020. Her role involves overseeing regulatory compliance and ensuring that clinical trials adhere to established guidelines. She has also served as a Clinical Trial Associate at Nutrasource since 2019, contributing to the management of clinical trials and supporting the research team in Guelph, Ontario. Her tenure at Nutrasource highlights her commitment to maintaining high standards in clinical research.
Previous Experience in Clinical Trials
Sandra Pacheco has extensive experience in clinical trials, having worked in various roles across multiple organizations. She served as a Sr. Clinical Trial Assistant at Quintiles in partnership with Hoffmann-La Roche Ltd. from 2014 to 2015. She held the position of Clinical Trial Coordinator at Novo Nordisk from 2016 to 2018 and worked as a Global Study Associate at AstraZeneca for 9 months in 2018. Additionally, she was an In-House CRA II at PRA Health Sciences dedicated to BAYER in 2016. This diverse experience has equipped her with a comprehensive understanding of clinical trial processes.
Long-Term Career in the Pharmaceutical Industry
Sandra Pacheco has over 25 years of experience in the pharmaceutical industry. Her career began at Schering-Plough Research Institute, where she worked as a Quality Control & Regulatory Affairs Assistant from 1991 to 2002. She later held positions at Novartis as a Quality Assurance Administrative Assistant from 2002 to 2010, and at Roche as a Clinical Trials Assistant from 2011 to 2014. This extensive background has provided her with a strong foundation in Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines.
Skills and Professional Attributes
Sandra Pacheco is recognized for her ability to complete assigned tasks efficiently and within project timelines. She demonstrates reliability, honesty, and integrity in her professional conduct. Her strong organizational skills enable her to manage multiple tasks and studies effectively in a fast-paced environment. These attributes contribute to her success in the clinical regulatory affairs field, where attention to detail and adherence to regulatory standards are critical.