Cassandre Noel
About Cassandre Noel
Cassandre Noel is a Senior Manager at Bristol Myers Squibb with extensive experience in quality control and clinical research.
Company
Cassandre Noel is currently employed at Bristol Myers Squibb, a leading global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines. Cassandre has held multiple roles within the company, showcasing a strong track record of expertise and growth in the field of quality control and materials management.
Title
Cassandre holds the title of Senior Manager at Bristol Myers Squibb. In this leadership position, Cassandre is responsible for overseeing various aspects of quality control and materials management, ensuring compliance with industry standards and regulatory requirements.
Education and Expertise
Cassandre Noel has a Master of Science (M.S.) in Biomedical Science from the University of Medicine and Dentistry of New Jersey (UMDNJ) and a Bachelor of Science (BS) in Biochemistry from Saint Elizabeth University. Cassandre has completed various professional training programs, including the Principles of Clinical & Translational Research in Oncology, and is certified as a Clinical Research Coordinator (CRC) through the CITI Program. Additional courses completed include the GCP for Clinical Trials, Shipping and Transport of Regulated Biological Material, and NIH Clinical Research Training Course.
Background
Cassandre Noel has a diverse professional background spanning over a decade, with experience in various roles related to research, quality control, and clinical trials. Prior to the current role at Bristol Myers Squibb, Cassandre has held positions such as Manager, QC Materials, Senior QC Scientist, Analytical Trainer, and Quality Control Scientist at the same company. Previous experience also includes roles at Skin Laser & Surgery Specialists of NY and NJ, Xeme Biopharma, Roche, University of Medicine and Dentistry of New Jersey, and other institutions.
Certifications and Courses
Throughout Cassandre's career, a commitment to continuous learning and professional development has been evident. Cassandre is certified as a Clinical Research Coordinator (CRC) through the CITI Program, has completed the GCP for Clinical Trials with Investigational Drugs and Medical Devices course, and has undergone training in the Shipping and Transport of Regulated Biological Material. Other professional development activities include the NIH Clinical Research Training Course and the NIDA Clinical Trials Network Good Clinical Practice Course.