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Vanessa MontanariVM

Vanessa Montanari

Clinical Research & Medical Strategy Consultant

€717/day
2 projects
Paris, FR
15+ years

Average response time: 1 hour

About Vanessa

I am the founder of Pharmaspecific, a clinical research organization with over 15 years of experience supporting pharmaceutical companies, CROs, and biotech organizations across Europe and internationally.

I specialize in bridging clinical research, real-world data (RWD/RWE), and medical communication, with strong expertise in oncology and complex therapeutic areas.

In parallel, I lead a pharmaceutical development initiative focused on plant-based therapeutics and GMP-compliant production, providing additional insight into regulatory strategy, product development, and healthcare innovation.

I support sponsors and partners across the full lifecycle of clinical and observational studies, including:

• Clinical trial support (Phase II–IV, observational studies)
• Patient engagement and recruitment strategies
• Real-world data collection and patient registries
• Medical writing and scientific communication
• Regulatory support (EU / France)
• Project management and CRO coordination

I work with a multidisciplinary team of physicians, clinical research professionals, and medical writers, enabling me to deliver both strategic insight and operational execution.

I am particularly engaged in projects involving:

• Real-world data and patient registries
• Rare diseases and patient-centric approaches
• Clinical strategy and study design
• Scientific and medical content for healthcare audiences

My approach combines scientific rigor, operational efficiency, and a strong focus on delivering actionable, high-quality outcomes.
  • English

    Fluent

  • French

    Native or bilingual

Remote only
Primarily works remotely

Experience

  • Zinga pharma
    Founder & Managing Director
    PHARMACEUTICALS INDUSTRY
    January 2024 - Today (2 years and 5 months)
    Tananarive, Madagascar
    Pharmaceutical development and manufacturing initiative focused on plant-based therapeutics and GMP-compliant production in Africa and overseas territories.

    Key responsibilities:

    • Development of GMP-compliant pharmaceutical manufacturing facilities (Madagascar & Caribbean)
    • Strategic positioning of plant-based therapeutics and phytomedicine
    • Regulatory alignment and market access strategy
    • Development of international partnerships (Europe / Africa)
    • Implementation of sustainable and local healthcare ecosystems

    Focus on bridging traditional medicine and modern pharmaceutical standards to support therapeutic innovation and access to care.
    Phytomedicine Pharmaceutical Development GMP Regulatory Strategy Healthcare Innovation
  • Pharmaspecific
    Founder and Director
    PHARMACEUTICALS INDUSTRY
    May 2010 - Today (16 years and 1 month)
    Champs-sur-Marne, France
    Clinical research organization providing full-service support to pharmaceutical companies, CROs, and biotech organizations.

    Key activities:

    • Clinical trial monitoring and coordination (Phase II–IV)
    • Project management of international studies
    • Patient reimbursement and site support
    • Regulatory submissions (ANSM, CNIL, ethics committees)
    • Medical writing and scientific documentation
    • Quality management (ISO 9001)
    • GCP audits

    Management of a multidisciplinary team including CRAs, study coordinators, and medical experts.
    Monitoring Formation Audit BPC Management de projet TEC

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Education

  • Master in cellular biology and physiology
    Paris 13 university
    2003
  • CRA certification
    Sup santé
    2004

Certifications

  • Coaching
    CNFDI
    2018

Skill set

Categories