Rosa Garrido
About Rosa Garrido
Rosa Garrido is a Senior Protocol Specialist at Bristol Myers Squibb in Sevilla, Andalucía, España, with extensive experience in clinical trials and corporate communication.
Title and Role at Bristol Myers Squibb
Rosa Garrido is currently positioned as a Senior Protocol Specialist at Bristol Myers Squibb in Sevilla, Andalucía, España. She plays a crucial role in the set-up, maintenance, quality review, and reconciliation of the electronic Trial Master File (eTMF). Rosa is responsible for managing vendor invoices and site payments, ensuring compliance and timely processing. Additionally, she supports health authority inspections and Clinical Quality Assurance (CQA) audits.
Previous Experience at Celgene
Before joining Bristol Myers Squibb, Rosa Garrido accumulated extensive experience at Celgene, where she held multiple roles over a period of seven years. She was a Senior Clinical Trial Associate from 2018 to 2019 and a Clinical Trial Associate (CTA) from 2016 to 2018. In these roles, she developed a new training program for Site Payments Management, leading to faster and more efficient onboarding of new CTAs. Earlier at Celgene, she served as Finance and Business Operations Coordinator from 2011 to 2016.
Early Career and Roles in Switzerland
Rosa Garrido's early career included significant roles in Switzerland. From 2005 to 2011, she worked at Lundin Petroleum as an EHS, Corporate Responsibility, Investor Relations Executive Assistant in Ginebra. Prior to that, she served as a Credit Department Assistant at HSBC from 2004 to 2005 and as a Translator and Conference Interpreter at Agenor from 2003 to 2004. These roles provided her with a broad skill set in corporate responsibility, investor relations, and financial operations.
Educational Background
Rosa Garrido holds a Máster en Dirección de Comunicación Corporativa from EAE Business School & Universidad de Barcelona, completed in 2014. She earned a Master's degree in E-Business, Marketing & Communication from Université de Geneve in 2010. Rosa also studied Language Interpretation and Translation at Universidad de Granada, where she completed her education in 2002.
Key Contributions and Responsibilities
At Bristol Myers Squibb, Rosa implemented a new study Start-up guide and a CTA Guide for ED studies, and fully trained and mentored three Clinical Trial Associates. She contributes to the operational execution of Phase I clinical studies across regions including the USA, Canada, Europe, and Japan. Rosa also conducts quality oversight of Contract Research Organization (CRO) teams and vendors, ensuring stringent adherence to quality standards.