Pauline Arbez Koga
About Pauline Arbez Koga
Pauline Arbez Koga is a Site Monitor with over 20 years of experience in clinical research and site monitoring, having worked at Pfizer and Bristol-Myers Squibb.
Current Position: Site Monitor
Pauline Arbez Koga is currently serving as a Site Monitor. With over two decades of experience, she plays a crucial role in overseeing clinical trials and ensuring compliance with regulatory standards and Good Clinical Practice (GCP) guidelines. Her responsibilities include the development and implementation of site monitoring plans and the oversight of trial sites to ensure the accuracy and integrity of clinical data.
Previous Experience at Pfizer
Pauline Arbez Koga worked as a Clinical Research Associate at Pfizer from 2001 to 2006. During her five-year tenure, she was involved in various clinical trials, predominantly focusing on oncology and immunology. Her work at Pfizer included ensuring regulatory compliance, monitoring site activities, and contributing to the overall success of clinical trials.
Role at Bristol-Myers Squibb
In her career, Pauline has also served as a Site Monitor for Bristol-Myers Squibb. Her role involved extensive site monitoring activities, ensuring adherence to protocol and regulatory requirements, and supporting the successful execution of clinical trials. Her contributions significantly influenced the quality and reliability of trial outcomes.
Academic Background: University of Manitoba
Pauline Arbez Koga completed her education at the University of Manitoba, where she studied from 1980 to 1984. Her academic training laid the foundation for her extensive career in clinical research and site monitoring, equipping her with the necessary skills and knowledge to excel in her field.
Expertise in Clinical Research and Site Monitoring
With over 20 years of experience, Pauline Arbez Koga has garnered substantial expertise in clinical research and site monitoring. She has worked on multiple clinical trials focusing primarily on oncology and immunology, developed and implemented site monitoring plans, and ensured compliance with regulatory standards. Additionally, she has played a key role in training and mentoring junior clinical research associates, sharing her extensive knowledge and experience to nurture the next generation of professionals in the field.