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Nina NguonNN

Nina Nguon

Medical & Clinical Affairs Leader Consultant

700 €/jour
Paris, FR
8-15 ans

Délai de réponse moyen : Quelques jours

À propos de Nina

GLOBAL MEDICAL AFFAIRS LEAD CONSULTANT
Clinical Evidence • Scientific Communication • Medical Strategy • Pharma • MedTech • 12+ years experience

I help pharma and medtech translate innovation into measurable medical impact worldwide.

CORE AREAS OF EXPERTISE
- Medical Strategy & Leadership – Global/local planning, governance, launch readiness, medical plans
- KOL & Scientific Network Development – Advisory boards, expert mapping, scientific partnerships
- Scientific Communication & Medico-Marketing – Content strategy, omnichannel materials, launches
- Medical Education & Events – Congresses, symposia, workshops, webinars, training platforms
- Clinical Development & Evidence Generation – Clinical trials, RWE, IIS, feasibility, vendor management
- Medical Writing, Publications & Documentation – Protocols, SOPs, medical materials, regulatory reports
- Patient Affairs – Ethics, informed consent, patient programs, patient data collection, enrollment
- Governance, Compliance & Quality – GCP, FDA/EMA, GDPR, MLR review

THERAPEUTIC & SCIENTIFIC AREAS
Medical Aesthetics • Dermatology • Oncology (MM, NSCLC, NETs, HCC) • Hematology • Rare Diseases • Infectiology • Neurology • Dentistry

PRODUCTS
Medical Devices • Pharmaceuticals • Biologics • Immunotherapy • Diagnostics

Available for freelance and consulting opportunities.
  • Anglais

    Capacité professionnelle complète

  • Français

    Bilingue ou natif

Accepte de travailler sur site
Paris (jusqu’à 50 km), Lyon (jusqu’à 50 km)

Expériences

  • SUISSELLE
    Global Scientific, Medical & Clinical Affairs Lead
    INDUSTRIE PHARMACEUTIQUE
    juillet 2024 - Aujourd'hui (1 an et 11 mois)
    Switzerland
    I lead the global Medical Affairs, Clinical strategy and operations for an international aesthetic medicine portfolio, with a focus on strengthening scientific credibility, and scaling medical impact across markets (EMEA, Asia, Latam).

    ▪ Transform the Global Medical Affairs strategy, and operational execution with commercial and brand milestones
    ▪ Lead global medical education programs and high-visibility scientific events, including major international congresses (IMCAS, AMWC, Dubai Derma).
    → 2025 brand event: 160 customers, 25 countries
    ▪ Lead evidence generation strategy, incl. clinical trials, RWE, investigator-initiated studies, and case series, supporting publication, vendor management
    ▪ Build a medical & scientific resource library to support medical education
    ▪ Drive KOL strategy and scientific network development, emerging leader programs, and long-term scientific partnerships
    ▪ Oversee medical information processes, ensuring accurate, referenced, and compliant responses
    ▪ Design and implement omnichannel scientific engagement strategies to support business development and market expansion
    ▪ Lead clinical evaluation of products, updates of regulatory documentation, responses to notified body and competent authorities
    ▪ Manage budget, contracts, and FMV negotiations
    ▪ Ensure compliance with internal policies, ethical standards, and codes of conduct, implementing and maintaining Medical Affairs SOPs

    Products & Scope
    Injectable aesthetics – Class III medical devices & Cosmetics
    • Skin & hair boosters (Cellbooster®)
    • Dermal fillers (HA – Apriline®)
    • Cosmetics (microneedling)
    Clinical Development Medical Education Symposium Evidence Generation Clinical Evaluation
  • SEPTODONT
    Global Medical Manager, Clinical Evaluation, Medical Affairs
    INDUSTRIE PHARMACEUTIQUE
    septembre 2023 - juillet 2024 (10 mois)
    Paris, France
    • Ensured internal and external scientific communication, reported competition data, supported publications initiatives
    • Presented medical scientific training & insights to R&D, marketing, regulatory teams
    • Reviewed promotional and non-promotional materials, managed claims, indication extensions, analyze efficacy and safety data
    • Acted as Medical Expert for the assigned brands/products for all medical inquiries & authorities challenge questions
    • Acted as Medical Lead to ensure CE/US market approval and compliance with business deliverables and regulatory affairs
    • Supported Medical Information requests, managed data generation and study design (investigator-initiated studies, registries, trials)
    • Managed HCPs and supported medical association partnerships, participate in medical congresses

    ------------------
    Implantable Medical Devices:
    Hemostatic sponge (Hemocollagene, Septodont)
    Post-extraction dressing (Alveogyl, Septodont)
    Endodontic cement (Endomethasone N/Endomethasone Liquid, Septodont)
    Dental membrane (R.T.R.+ Membrane, Septodont)
    Medical Writing Regulatory Compliance Medical Devices Congress Revue de littérature
  • COLGATE-PALMOLIVE
    Global Senior Medical Communication Manager, Medical Affairs Dermatology | Aesthetic Medicine
    INDUSTRIE PHARMACEUTIQUE
    septembre 2021 - décembre 2022 (1 an et 3 mois)
    Paris, France
    • As medical expert and lead, fully delivered the global medical communication plans & publications strategy
    • Designed and disseminated innovative content in traditional/digital media & education platform, provided toolbox and guidelines
    • Trained commercial & business team in EU, US, Latam, responded to medical and reviewer questions on products
    • Drove 3 R&D publications that were published in peer-reviewed journals, significantly increased scientific credibility of brands
    • Identified world-renowned HCPs to build an international advisory board for regular expert meetings
    • Engaged key experts and scientific societies to communicate key message externally in congress, symposia, webinars
    • Influenced cross-functional teams (Marketing, Business, R&D, Clinical, Regulatory, vendors) that resulted in full project compliance
    Symposium Medical Review Promotional Materials Advisory Board

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Formations

  • EU Medical Device Regulation
    2023
    EU Medical Device Regulation
  • PhD Life Sciences, Chemical burns and wound healing
    University of Grenoble-Alpes
    2013
    Doctorate

Certifications

  • Patient Engagement
    Wecan
    2025
    Patient affairs Patient advocacy Patient engagement Patient expérience evidence
  • ICH-E6 Good Clinical Practices
    NIDA
    2025
    FDA ICH GCP Clinical Trials

Compétences

Catégories