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Bruno PouzetBP

Bruno Pouzet

Consultant drug discovery strategies

€1,000/day
Copenhagen, DK
15+ years

Average response time: 1 hour

About Bruno

I am a consultant expert in project management and group reorganisation with a strong industrial background in drug discovery and preclinical strategies.
I gained specific expertise as a project manager and consultant in outsourcing, leadership, consulting, and project management activities, in large international pharmaceutical companies, as well as in my own consultancy specializing in project management and outsourcing solutions.
Driven by a passion for innovation and ventures, I am dedicated to advancing drug and technology projects that have the potential to significantly improve patient treatment outcomes and quality of life. My ability to navigate complex challenges and foster cross-disciplinary collaboration makes me a valuable resource in developing projects within the pharmaceutical industry.
  • English

    Native or bilingual

  • French

    Native or bilingual

  • Danish

    Conversational

Can work on-site
Copenhagen (up to 50km), Odense (up to 10km), Aarhus (up to 10km), Malmo (up to 10km), Lund (up to 10km)

Experience

  • Saveurs de France ApS
    Ownwer - Director
    E-COMMERCE
    January 2018 - Today (8 years and 5 months)
    Copenhague, Denmark
    I founded and developed a business specialized in the importation and sales of French delicacies from small producers, which I turned into a profitable venture. I achieved a 116% increase in profitability through three recent strategic adjustments—product selection, pricing, and sales channels. This obtained during a period of high inflation. I managed the entire supply chain, marketing, sales, logistics, and ensured strict compliance with Danish regulations specific to food and alcoholic beverages. Now that this business is on the safe way, I can work further on freelance consulting in the drug discovery domain.
    Shopify E-commerce Retail Commercial strategy Logistics
  • BeVivo GmbH
    Owner - Director
    CONSULTING AND AUDITS
    January 2013 - January 2021 (8 years)
    Basel, BS, Switzerland
    I developp preclinical strategies for R&D organizations across various projects in psychiatry, degenerative diseases, and inflammation. For these projects, I provided preclinical strategies, selected CROs from my database, and supervised of outsourced studies. My clients included academic researchers, start-ups, and international pharmaceutical companies.

    More specifically, tasks supported from my agency included:
    • Project management consulting, preclinical strategy, compound prioritization, and project evaluation, leveraging the most advanced technologies.
    • Facilitating connections with relevant Key Opinion Leaders (KOLs).
    • Supporting R&D organizations in developing strategies to ensure the successful progression of compounds and to prepare for out-licensing processes in a french pharmaceutical company.
    • Advising biotechs and pharmaceutical companies in reorganizing their preclinical infrastructures to optimize cost efficiency, internal resource utilization, and ensure a smooth transition between preclinical and clinical phases.

    Some examples of concrete projects performed for clients:
    • Evaluating the in vitro and in vivo consequences of mRNA constructs on cells and motoneurons. This was outsourced for a Swiss biotech to a French CRO. I found the partner, implemented the contract, and oversaw the study up to the final report.
    • Supporting the commercial development of two CROs: enhancing visibility, prioritizing investments, and acquiring new clients.
    • Evaluating the in-Vivo and ex-Vivo consequence of food supplements on the response of the immune system of mice contaminated with Influenza A virus. It was performed for a Swiss biotech in a French CRO under my supervision.
    • Designing a preclinical strategy for a major German pharmaceutical company aiming at evaluating the potential of compounds against cognitive disorders. The strategy included to list the CROs to perform studies, and selecting KOLs.
    Outsourcing Project Management Preclinical Strategic planning Audit
  • F. Hoffmann-La Roche AG
    Group leader, Project leader.
    PHARMACEUTICALS INDUSTRY
    January 2009 - January 2011 (2 years)
    Basel, BS, Switzerland
    At Hoffmann-La Roche, as a Group Leader, I led and reorganized a team of four PhD scientists and 15 technicians in Basel, as well as a smaller team in California. Together with selected external partners (CROs and academics), I built and maintained a highly efficient team to support numerous internal projects.
    I designed and oversaw the implementation of in-vivo workflows that enabled approximately 10 transitions of "clinical lead series" or "entry into GLP tox" within the CNS pipeline over three years. My teams and I also developed translational models for late-stage compounds, resulting in three entries into human studies (EIH) over two years. My work involved preclinical efficacy and toxicology studies across various animal species, from rodents to mini-pigs.
    As project leader, I recovered a project in the domain of cognitive dysfunction, by reorganizing the working group and defining achievable goals in line with time-lines given by the scientific executive management. It included the writing of monographs, and chapters for investigator brochures.
    In collaboration with the IT department we developed an electronic lab-book system to move from paper books to an electronic GLP approved system.
    Project Management Drug Discovery line management Preclinical Reporting

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Education

  • Post-graduated master in
    ROYAL DANISH SCHOOL OF PHARMACY COPENHAGEN
    2002
    Post-graduated master in
  • PhD
    ETH ZÜRICH
    1999
    PhD

Certifications

  • IPMA D
    VZPM Zürich
    2013

Skill set

Categories