Laura Rodriguez
About Laura Rodriguez
Laura Rodriguez is a Clinical Site Manager at Bristol-Myers Squibb with over 15 years of experience in clinical site management and a strong background in clinical research.
Title
Laura Rodriguez currently holds the position of Clinical Site Manager at Bristol-Myers Squibb. Her role involves overseeing clinical trial sites, ensuring compliance with regulatory requirements, and managing site performance.
Company
Laura Rodriguez has been employed by Bristol-Myers Squibb for over 15 years. During her tenure, she has been responsible for the management and operational oversight of clinical trial sites, contributing significantly to the company's research and development efforts.
Education and Expertise
Laura Rodriguez graduated from the University of Buenos Aires, where she studied from 1996 to 2002. She possesses over 15 years of professional experience in clinical site management, bringing a wealth of knowledge to her current role at Bristol-Myers Squibb. Her educational background and extensive experience underline her expertise in clinical research.
Background
Laura Rodriguez began her career in clinical research in 2004, initially working as a Clinical Research Associate (CRA) at Pfizer for one year. She then spent three years at Organon, continuing her role as a CRA. Her experience spans various pharmaceutical companies, providing her with a robust understanding of the field.
Clinical Research Experience
With over 15 years of experience, Laura Rodriguez has established herself as a knowledgeable professional in clinical site management. Her career includes roles at Pfizer, Organon, and Bristol-Myers Squibb, where she has demonstrated a strong capacity for managing clinical trials and ensuring site compliance with industry standards.