Adriana Mejia
About Adriana Mejia
Adriana Mejia is a Clinical Site Monitor at Bristol-Myers Squibb with over 7 years of experience in clinical monitoring and coordination.
Title
Adriana Mejia is currently employed as a Clinical Site Monitor at Bristol-Myers Squibb, a prominent biopharmaceutical company.
Professional Background at Bristol-Myers Squibb
Adriana Mejia has been working as a Clinical Site Monitor at Bristol-Myers Squibb since December 2016. In this role, she is responsible for overseeing clinical trial sites, ensuring compliance with regulatory requirements, and maintaining high standards of quality control.
Previous Experience at ICON PLC
Prior to her current position, Adriana Mejia held the role of Clinical Trial Assistant at ICON PLC for a brief period in 2016. During her four-month tenure, she assisted in the administrative aspects of clinical trials, supporting the coordination and documentation processes.
Role at Riesgo de Fractura S.A. Cayre IPS
From 2011 to 2016, Adriana Mejia worked as a Study Coordinator at Riesgo de Fractura S.A. Cayre IPS. Over her five-year tenure, she coordinated clinical studies, managed patient recruitment and follow-ups, and ensured the smooth operation of research projects.
Education and Expertise from Universidad Colegio Mayor de Cundinamarca
Adriana Mejia completed her studies at Universidad Colegio Mayor de Cundinamarca, where she studied from 2005 to 2009. Her education has bolstered her expertise in clinical monitoring and coordination, contributing to her over 7 years of professional experience in the field.