Sophie Gayot
About Sophie Gayot
Sophie Gayot is a Local Trial Coordinator at SynTech Research, where she has worked since 2017. She has a background in biology and project management, with previous roles at PRP Technologies and Nestlé.
Work at SynTech Research
Sophie Gayot has been employed at SynTech Research since 2017, serving as Chargée de clientèle BPE and Local Trial Coordinator. In this role, she is responsible for ensuring compliance with internal operating procedures and BPE standards in trial coordination. Her duties include writing detailed BPE trial reports and engaging in regulatory monitoring. She also plays a key role in the centralization of outsourced analyses, contributing to the efficiency and effectiveness of trial management.
Previous Experience at PRP Technologies
Prior to her current position, Sophie Gayot worked at PRP Technologies from 2014 to 2016 as Ingénieur Chef de Projets R&D. During her two years in Bréhan, France, she focused on research and development projects, contributing her expertise to the advancement of the company's objectives.
Educational Background
Sophie Gayot studied at Université François Rabelais de Tours, where she earned a Licence in Biologie from 2006 to 2009. She furthered her education at Université d'Angers, achieving a Master 2 (M2) in Technologies du Végétal et Productions Spécialisées from 2009 to 2011. This educational foundation has equipped her with the necessary skills for her roles in research and trial coordination.
Professional Experience in Research
Sophie Gayot has a diverse background in research roles. She worked at Nestlé as Assistante de recherche for six months in 2011, and at Inra - Institut national de la recherche agronomique as Ingénieur d’études en Biologie Moléculaire from 2012 to 2013. Additionally, she served as Assistante de sélection at Enza Zaden for four months in 2010. These positions have contributed to her expertise in trial coordination and data management.
Technical Expertise
Sophie Gayot possesses expertise in using ARM software for creating trial protocols and managing trial data. Her technical skills support her responsibilities in trial coordination and compliance with BPE standards. She engages in the management of internal operating procedures, ensuring that all processes align with regulatory requirements.