À propos de Clémentine
Français
Bilingue ou natif
Anglais
Capacité professionnelle complète
Expériences
- ASIT BiotechScientist in Production/R&D departmentINDUSTRIE PHARMACEUTIQUEfévrier 2015 - octobre 2016 (1 an et 8 mois)BelgiumDevelopment and improving of process for new products; planning and execution of API production (Downstream processing) at lab and pilot scale according to QC ans pre-(clinical) needs; Transfer and up-scaling to GMP facilities; writing and revison of production SOP's; Evaluation of day to day GMP scale planning, evaluation IPC decision level (GO/NO GO, important, informative...), choice and test of equipments for GMP scale production, writing technical documentation and follow up with CMO productions
- ASIT Biotech (formerly Biotech Tools)Senior Project LeaderINDUSTRIE PHARMACEUTIQUEoctobre 2016 - mars 2017 (5 mois)BelgiumResponsabilities :Coordinating the production and the analytical developement of 2 projects; Design and execution of the production protocols to improve the yield and the reliability, responsible of the compliance with the planningKey assignements:Development and improving of process for new products; planning and execution of API production (Downstream prossecing) at lab and the pilot scale according to QC and (pre-)clinical needs; Choice and test of equipment for GMP scale production
- Pharmaxess ConsultingValue & Access Strategy ConsultantCONSEIL & AUDITseptembre 2024 - Aujourd'hui (1 an et 8 mois)BelgiumAdvise biotech companies on market access strategy, value communication, and competitive positioning. Conduct pricing and market access analyses across EU and US markets, including payer segmentation, CMS reimbursement pathways, and competitive price benchmarking. Develop evidence generation and value demonstration roadmaps, integrating payer, clinician, and patient insights to guide development decisions. Provide strategic guidance to leadership and investors, articulating how scientific differentiation translates into market and reimbursement value. Participate in and provide strategic input to the translation and adaptation of French HTA dossiers into Belgian submissions, ensuring alignment with local frameworks and payer evidence needs.
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Formations
- Gross-To-Net training seriesInforma connect2024Gross-To-Net training series
- EUMAUD|Market Access Society2024EUMAUD