Marie Biet
About Marie Biet
Marie Biet is a Regional Clinical Trial Management Associate at BeiGene with extensive experience in managing clinical trials across multiple phases and therapeutic areas.
Current Role at BeiGene
Marie Biet is currently working as a Regional Clinical Trial Management Associate at BeiGene, a biotechnology company focused on developing innovative drugs for cancer treatment. In her role, she manages clinical trials remotely, ensuring efficient trial operations and adherence to protocols.
Previous Experience at ICON plc
Marie Biet worked as an In-house Clinical Research Associate at ICON plc, a global provider of outsourced drug and device development and commercialization services. From 2020 to 2022, she was based in the Greater Paris Metropolitan Region, where she handled various aspects of clinical trial operations, including study planning and coordination.
Positions at Institut du Cerveau – Paris Brain Institute
Marie Biet spent several years at the Institut du Cerveau – Paris Brain Institute. From 2018 to 2020, she was a Clinical Project Manager in Ville de Paris, Île-de-France, France. Prior to that, she served as a Study Coordinator from 2017 to 2020. During her tenure, she was involved in managing clinical trials and research projects in the fields of neurology and psychiatry.
Extensive Academic Background
Marie Biet has an extensive academic background in both the sciences and business. She earned a Bachelor's degree in Biological Sciences from Paris-Sud University and Ecole normale supérieure. She also holds a Master's degree in Management from EDHEC Business School and a Master in Marketing from Thammasat University. Additionally, she obtained a Clinical Research Associate Certificate through the ARC.INTENSE Program in 2017.
Expertise in Clinical Trials and Therapeutic Areas
Marie Biet has managed clinical trials across multiple phases, including Phase Ib, IIa, IIb, and III. She has extensive experience in diverse therapeutic areas such as Oncology, Hematology, Neurology, Genetics, and Rare Diseases. Her responsibilities have included study planning, design, start-up/conduct, site management, vendor and CRO management, budget and contract management, and system design. She is well-versed in clinical operations and Good Clinical Practice (GCP).