Marion Laborie has a diverse work experience in the field of clinical project management and research. Marion currently holds the position of Clinical Project Manager at Sensorion, starting from March 2021. Prior to this, they worked as a Clinical Project Manager at Clinact (via TempoPHARMA) from January 2021 to February 2021.
Marion also gained extensive experience at Inventiva Pharma (via TempoPHARMA), where they served as Lead Clinical Project Manager from May 2020 to December 2020, and as a Clinical Project Manager from November 2019 to December 2020.
Earlier in their career, they worked as a Junior Clinical Project Manager at NEOVACS SA from March 2019 to November 2019. Before that, they worked at NEOVACS as a Clinical Study Coordinator from March 2015 to February 2019, and as a Clinical Research Associate from June 2011 to February 2015.
Marion also has experience as an Engineer Assistant and Research Assistant during their earlier years in the field. Marion'sroles encompassed various responsibilities including clinical project management, quality control/assurance, vendor management, budget management, timeline management, review of study data, development of SOPs, and support in site and CRO audits. Marion has a solid understanding of international clinical trials.
Marion LABORIE's education history is as follows:
- In an unspecified year, Marion attended Clinfile and completed a one-day course in Easy Study Management (ESM, CTMS) in Sèvres.
- Also in an unspecified year, Marion attended ProductLife Group and completed a one-day course in Harmonized Review Process of Regulation for Multinational Clinical Trials in Paris.
- In an unspecified year, Marion attended CeNGEPS and completed a one-day course in "Système d’information et de gestion de la Recherche et des essais cliniques" in Paris.
- In an unspecified year, Marion attended CEFIRA and completed a three-day program in Biostatistics with R in Paris.
- In an unspecified year, Marion attended IRSN and received a Certification of Competent Person for Radiation Protection after completing a two-week course in Fontenay Aux Roses.
- In an unspecified year, Marion attended Matrix Consulting and completed a five-day course in English effective scientific writing in Paris.
- From 2002 to 2003, Marion attended Pierre and Marie Curie University and earned a post-master degree in R & D Biotech. The program lasted for five years after graduation and covered subjects such as Biotechnology, Immunology, Cell Biology, Molecular biology, Bioethics, and Quality.
- From 2001 to 2002, Marion attended Université Paris-Est Créteil (UPEC) and earned a Master of Science in Cellular Biology and Animal Physiology. The program focused on Immunology, Molecular biology, Cell signaling, Genetics, Enzymology, and Microbiology.
- In 2012, Marion returned to ProductLife Group in Paris to go through Harmonized Review Process of Regulation for Multinational Clinical Trials. The completion year is not specified.
These are all the educational experiences that can be derived from the provided information.
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