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Clémentine LaurentCL

Clémentine Laurent

Value & Access Strategy Consultant

780 €/jour
Liège, BE
8-15 ans

Délai de réponse moyen : 1h

À propos de Clémentine

I help biotech companies and investors structure and maximize the value of their innovations from early development through a Value & Access strategy that bridges science and business.

With a scientific background and over ten years of experience in biotech, I combine deep product insight across technical development, regulatory affairs, non-clinical and clinical stages with a strong business mindset and strategic agility. This 360° perspective enables me to translate complex science into actionable, value-driven strategies.

Over the past five years, I have specialized in Market Access and Value Strategy for innovative therapies and drug–device combinations, helping early-stage teams and investors to shape their value story, anticipate payer and stakeholder expectations, and optimize development priorities.

My approach integrates:

Market and stakeholder potential assessment

Insight generation and strategic positioning

Definition of value propositions and competitive differentiation

Alignment of science, patient needs, and payer value

Realistic pricing and market access strategies that enhance both clinical impact and investment return
  • Français

    Bilingue ou natif

  • Anglais

    Capacité professionnelle complète

Accepte de travailler sur site
Liège (jusqu’à 50 km)

Expériences

  • ASIT Biotech
    Scientist in Production/R&D department
    INDUSTRIE PHARMACEUTIQUE
    février 2015 - octobre 2016 (1 an et 8 mois)
    Belgium
    Development 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
    Gestion de projet
  • ASIT Biotech (formerly Biotech Tools)
    Senior Project Leader
    INDUSTRIE PHARMACEUTIQUE
    octobre 2016 - mars 2017 (5 mois)
    Belgium
    Responsabilities :
    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 planning
    Key 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
    Gestion de projet
  • Pharmaxess Consulting
    Value & Access Strategy Consultant
    CONSEIL & AUDIT
    septembre 2024 - Aujourd'hui (1 an et 8 mois)
    Belgium
    Advise 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.
    Pricing Market Access life sciences investment

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Formations

  • Gross-To-Net training series
    Informa connect
    2024
    Gross-To-Net training series
  • EUMAUD
    |Market Access Society
    2024
    EUMAUD

Compétences

Catégories