Elsa Guzman Bonilla
About Elsa Guzman Bonilla
Elsa Guzman Bonilla is a Senior Clinical Trial Assistant at Aimmune Therapeutics with extensive experience in clinical research and trial management. She has worked in various roles across multiple companies, including Rigel, Genentech, and Gilead Sciences, and holds a Certificate in Clinical Trials Conduct and Management from UC Berkeley Extension.
Work at Aimmune Therapeutics
Elsa Guzman Bonilla has been employed at Aimmune Therapeutics as a Senior Clinical Trial Assistant since 2016. In this role, she has contributed to the management and oversight of clinical trials, ensuring compliance with regulatory standards. Her responsibilities include supervising data collection and review processes, as well as resolving quality control findings. She has played a significant role in leading a team of Clinical Trial Assistants, enhancing the efficiency and accuracy of trial operations.
Previous Experience in Clinical Research
Before joining Aimmune Therapeutics, Elsa Guzman Bonilla held several positions in clinical research. She worked at Rigel as a Clinical Research Coordinator from 2008 to 2010 and served as a Senior Research Associate from 2006 to 2008. Additionally, she was a Senior Clinical Trial Assistant at Alvine Pharmaceuticals Inc from 2012 to 2015 and at Dynavax Technologies from 2011 to 2012. Her experience also includes a role as a Global Studies Associate at Genentech from 2010 to 2011 and as a Consulting Clinical Project Assistant at Gilead Sciences from 2015 to 2016.
Education and Expertise
Elsa Guzman Bonilla has a solid educational background in clinical trials and biochemistry. She studied at UC Berkeley Extension, where she obtained a Certificate in Clinical Trials Conduct and Management from 2009 to 2010. She is currently pursuing an MBA Online Program at Universidad Rey Juan Carlos. Elsa also holds a Bachelor of Science in Biochemistry from Universitat de les Illes Balears, which she completed from 1997 to 2001. Her education complements her extensive experience in clinical research and trial management.
International Trial Experience
Elsa Guzman Bonilla possesses international trial experience, having worked with regulatory compliance across multiple regions, including North America, South America, Europe, Australia, and Africa. This experience enhances her ability to navigate diverse regulatory environments and contributes to the successful execution of global clinical trials. Her fluency in both English and Spanish further facilitates communication in various clinical trial settings.
Technical Skills and Contributions
In her roles, Elsa Guzman Bonilla has demonstrated proficiency in applying algorithms and AI/ML-based techniques to analyze large data sets. She has designed various clinical study forms to collect subject data as required by study protocols. Additionally, she has presented metrics to upper management regarding trial master file completeness, showcasing her ability to communicate critical information effectively.