Jessica Thomas
About Jessica Thomas
Jessica Thomas is a Global Trial Manager at Bristol Myers Squibb with over 15 years of experience in the clinical research and pharmaceutical industry.
Current Role at Bristol Myers Squibb
Jessica Thomas is engaged as a Global Trial Manager, working within the Global Clinical Trial Strategy & Operations, Late Development sector at Bristol Myers Squibb. Based in Durham, NC, she leverages her extensive experience to oversee and manage late-phase clinical trials. Her role involves developing strategies to enhance trial efficiency and compliance, ensuring adherence to Good Clinical Practice (GCP), and driving studies from initiation to completion.
Previous Experience at Parexel Biotech
Before her current role, Jessica Thomas served as a Project Leader at Parexel Biotech from 2011 to 2021. Over the span of a decade, she honed her skills in project management within the biotech sector. Her responsibilities likely included overseeing clinical trials, managing project timelines and budgets, and ensuring regulatory compliance. This tenure provided her with a robust foundation in managing complex clinical studies and coordinating cross-functional teams.
Background in Clinical Research and Regulatory Affairs
Jessica Thomas has amassed over 15 years of experience in the clinical research and pharmaceutical industry. Her early career includes roles such as Clinical Regulatory Specialist at PPD and Sr Regulatory Specialist at i3 Research. Additionally, she served as a Clinical Study Associate at GlaxoSmithKline, reinforcing her expertise in clinical monitoring and regulatory compliance. Her trajectory in various positions highlights her adeptness in navigating the regulatory landscape and ensuring GCP adherence.
Educational Background at North Carolina Central University
Jessica Thomas completed her academic studies at North Carolina Central University. While specific details regarding her degree or field of study are not provided, her education has evidently supported her extensive career in clinical research and project management. The knowledge and skills gained during her time at the university have played a crucial role in shaping her professional journey.
Specialization in Late Development Phases of Clinical Trials
Jessica Thomas specializes in the late development phase of clinical trials. Her current and previous roles have equipped her with in-depth knowledge and experience in managing late-stage clinical trials, which are critical in determining the efficacy and safety of new treatments before they reach the market. Her expertise likely includes developing and implementing study protocols, coordinating with various stakeholders, and ensuring compliance with regulatory requirements.