Marie Chantal Bonhomme
About Marie Chantal Bonhomme
Marie Chantal Bonhomme serves as the Associate Director of Reporting and Publishing at Celerion, where she has worked since 2020. With a strong background in clinical research and reporting, she has held various roles in the industry for over two decades, demonstrating expertise in regulatory compliance and project management.
Work at Celerion
Marie Chantal Bonhomme has been serving as the Associate Director of Reporting and Publishing at Celerion since 2020. In this role, she leads the preparation of clinical study reports, ensuring compliance with protocols, standard operating procedures, regulatory requirements, and good clinical practices. She monitors project management from start-up to completion, overseeing clinical reports and efficiency improvement projects. Additionally, she has established new corporate standards for electronic reporting and filing in line with updated regulatory guidelines.
Previous Experience in Clinical Research
Prior to her current position, Bonhomme worked at Celerion as Senior Global Reporting Manager from 2010 to 2020. Her career in clinical research began at MDS Pharma Services, where she held multiple roles including Reporting Manager, Team Leader, and Senior Pharmacokinetic Scientist from 2002 to 2010. She also gained experience as a Research Associate at CHUM and INSERM, contributing to her extensive background in clinical research operations.
Education and Expertise
Marie Chantal Bonhomme holds a Master of Science degree in Biomedical Sciences and a Bachelor of Science degree in Biological Sciences from Université de Montréal. She has a Lean Sigma Green Belt Certification, indicating her proficiency in process improvement methodologies. Bonhomme has also attended a DIA course on Regulatory Affairs, further enhancing her knowledge in this area, particularly concerning regulatory eCTD standards for FDA, EMEA, and TPD submissions.
Leadership and Training
In her current role, Bonhomme is responsible for hiring, training, guiding, and evaluating clinical reporting staff, providing both technical and organizational leadership. She prepares and conducts scientific training and presentations, showcasing her expertise in clinical research. Her strong aptitude for driving innovation and change is evident in her ability to make informed decisions that enhance clinical research operations.
Client and Project Management
Marie Chantal Bonhomme supports business development by engaging with clients to define their expectations and present the company's capabilities. She ensures client satisfaction while assisting commercial operations with budgetary control, including managing costs, overheads, and resources. Her role encompasses comprehensive project management, ensuring that all aspects of clinical studies are executed efficiently and effectively.