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Philippe GentinePG

Average response time: 1 hour

Freelancer profile translated to English.
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About Philippe

Pharmacist and holder of a PhD in Life Sciences, I have 15 years of experience in R&D, mainly in the pharmaceutical and biotech industries. Since 2019, I have been working as an independent consultant.

As an independent consultant, I support life science companies in analyzing, developing, and valorizing their innovations by addressing scientific, technological, regulatory, and medical-scientific issues.

My rigorous and tailor-made approach adapts to the specific needs of each client, integrating, if necessary, cross-functional dimensions: regulatory, industrial, or medical support. I offer personalized services, remotely or on-site, with responsiveness, clarity, and rigor.

My target therapeutic areas and specialties are as follows:
Main: vaccine, inflammation/immunology, oncology, infectious diseases
Complementary: rare diseases, medical devices, cosmetics, food supplements...

My service offering includes:
  • Conducting a scientific/technological state of the art;
  • Writing scientific & technical documents: study reports, scientific articles, responses to health authorities/review of registration dossiers...;
  • Scientific support for R&D tax credits;
  • Research and identification of new products, targets, processes, or innovation pathways;
  • Implementation of product candidate development strategy;
  • Project management;
  • Providing expertise in CMC activities;
  • Strategic analysis & evaluation of R&D projects;
  • Providing technical assistance;
  • Implementing strategic watch: scientific, technological, competitive, regulatory.
My rate is adjustable according to the duration and scope of the mission.

Do not hesitate to contact me for more information or for a future collaboration.
  • French

    Native or bilingual

  • English

    Fluent

Can work on-site
Antibes (up to 50km), Paris (up to 100km), Lyon (up to 100km), Montpellier (up to 100km), Nice (up to 100km)

Experience

  • PG Consulting (self-employed)
    Scientific and Strategic Consultant - Life Sciences
    PHARMACEUTICALS INDUSTRY
    August 2019 - Today (6 years and 10 months)
    Strasbourg, France
    As an independent consultant, I support life science companies in analyzing, developing, and valorizing their innovations by addressing scientific, technological, regulatory, and medical-scientific issues.

    **My service offering includes**:
    • Conducting a scientific or technological state-of-the-art;
    • Writing scientific & specific documents: R&D tax credit technical file, study reports, research project proposals, peer-reviewed scientific articles, slides for oral presentations, scientific review...;
    • Research and identification of new products, targets, processes, or innovation pathways;
    • Implementation of product candidate development strategy: Support in the Discovery phases, Identification of unmet medical needs, Market analysis, technological positioning and competitive environment analysis, Definition of the Target Product Profile (TPP), Support for CMC and non-clinical program development, Participation in guiding clinical development projects for new products, Conducting a gap analysis...;
    • Management, supervision & coordination of projects;
    • Providing expertise in CMC activities;
    • Strategic analysis & evaluation of R&D projects;
    • Providing technical assistance;
    • Implementing strategic watch: scientific, technological, competitive, regulatory watch.

    Main targeted therapeutic indications:
    Vaccines, Inflammation/Immunology, Oncology, Infectious Diseases
    Others: Rare diseases, Homeopathy, Cosmetics (hygiene products, makeup, skin care, sun products), medical devices (nasal sprays, chronic constipation treatment, bandages, implants, orthoses, catheters), food supplements
    Strategic Watch Writing Consulting Technological Positioning R&D Strategy
  • Projet de création de startup (BoostVax)
    Project Lead
    BIOTECH
    January 2018 - July 2019 (1 year and 7 months)
    Besançon, France
    The BoostVax project focused on the development of subunit vaccines based on protein and peptide targeting infectious and cancerous diseases in human and animal health.

    **First targets**: Bovine Babesiosis & Human Lung Cancer
    • Development of an innovative technology based on chemical modification of protein and peptide antigens, conferring unique properties and inducing an immune response up to 1000 times more potent;
    • Development of business plans & business models. Market and feasibility studies. Fundraising. Intellectual property strategy management. Building strategic partnerships. Team management. R&D project management: Production of an experimental vaccine against bovine babesiosis by B. divergens & Development of the BoostVax technology. Definition, development, and implementation of research strategies. Design, management, interpretation, and valorization of scientific studies. Determination of proof of concept (POC).
    Project Management Biotechnology R&D Start-up Vaccine
  • Baccinex, CDMO
    Pharmaceutical Project Coordinator
    PHARMACEUTICALS INDUSTRY
    September 2017 - December 2017 (4 months)
    Courroux, Switzerland
    Baccinex is a pharmaceutical laboratory specializing in the aseptic manufacturing of sterile liquid and lyophilized dosage forms
    • Main interface between the client and internal departments to ensure optimal project progress;
    • Implementation of preliminary activities for the production of clinical batches: Project feasibility study, Elaboration of price quotes, Drafting of the statement of work (SoW), Collection and review of technical information necessary for the successful completion of the project, Participation in pharmaceutical development tests for technical batches (retention test, filling test, lyophilization cycle optimization, shear test), Writing technical reports, Organization of clinical batch production;
    • Daily monitoring of ongoing projects.
    Outsourcing Pharmaceutical Production Project Coordination GMP

Reviews

4.8

Out of 4 ratings

F

Florence

Sanofi Pasteur

Reviewed on 4/20/2022

Very positive experience with Philippe who perfectly understood the objectives, asked the right questions to refine the scope, proposed research avenues, delved into a large volume of documentation and delivered a complete and structured report, all within the given deadlines.
F

Florence

Sanofi Pasteur

Reviewed on 8/1/2023

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Education

  • PhD in Life Sciences
    University of Strasbourg (UdS)
    2013
    Spécialisation en Vaccinologie
  • PharmD
    University of Strasbourg (UdS)
    2008

Skill set

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