Ruth Larbre
About Ruth Larbre
Ruth Larbre is a Clinical Site Manager at Bristol-Myers Squibb with over 17 years of experience in clinical research and regulatory affairs.
Title: Clinical Site Manager
Ruth Larbre currently holds the position of Clinical Site Manager at Bristol-Myers Squibb. In this role, she oversees the coordination and management of clinical trial sites to ensure compliance with regulatory standards and effective execution of clinical research studies. Her responsibilities include working closely with clinical investigators, managing site performance, and ensuring high standards of clinical data quality.
Company: Bristol-Myers Squibb
Ruth Larbre is presently employed at Bristol-Myers Squibb, a global biopharmaceutical company. At Bristol-Myers Squibb, she contributes her expertise in clinical research and site management to support the development and delivery of innovative medical treatments. Her role as a Clinical Site Manager involves ensuring that clinical trials are conducted efficiently, ethically, and in compliance with all regulatory requirements.
Previous Experience: Klinikum Rechts der Isar
From 2015 to 2016, Ruth Larbre worked as a Projektmanager - 1 Med Kardiologie at Klinikum Rechts der Isar der Technischen Universität München. During her one-year tenure, she managed cardiology projects, contributing to the development and oversight of clinical research initiatives within the medical facility.
Previous Experience: Premier Research
Ruth Larbre was employed at Premier Research from 2012 to 2015. Here, she served as a Start-Up Manager and Senior Clinical Research Associate (SCRA). In this capacity, she managed the initial phases of clinical trials, coordinated site start-up activities, and played a crucial role in ensuring the successful execution of research projects.
Background in Clinical and Regulatory Affairs
Ruth Larbre's career in the healthcare industry commenced in 2004 when she joined Danone as a Junior Scientific Engineer. Over the years, she has accumulated over 17 years of experience in clinical research and regulatory affairs. Her career trajectory includes roles at MedPass International, Covidien, and Premier Research, where she held various managerial positions. She has expertise in both the medical device and pharmaceutical sectors, managing clinical and regulatory affairs projects across different companies.