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Clinical Research Coach

Clinical Research Coach

Auteur(s): Leanne Woehlke
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The Clinical Research Coach Podcast bridges conversations between industry, thought leaders and patients. We have vulnerable and real conversations with the goal of impacting the industry in meaningful ways.Leanne Woehlke Science Sciences biologiques
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  • Julio Martinez-Clark- Bringing Cutting Edge Treatments to New Populations and Continents
    Jul 15 2025

    What does it take to bring cutting-edge research to new populations—and new continents?

    In this episode of The Clinical Research Coach, Leanne sits down with Julio Martinez-Clark, CEO of bioaccess®, to talk about why Latin America—especially Colombia—is becoming a prime destination for clinical trials. Julio shares insights into navigating regulatory pathways, building trusted networks, and designing trials that are both scientifically rigorous and locally relevant.

    Whether you're exploring new geographies or simply curious about how patient-centric research is evolving globally, this conversation will broaden your perspective.


    To Learn More:

    Julio Martinez Clark:

    https://www.linkedin.com/in/juliomartinezclark/

    bioaccess

    https://www.bioaccessla.com/


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    36 min
  • Disrupting Drug Development – Nasha Fitter’s Mission to Transform Rare Disease Research
    May 26 2025

    In this episode of The Clinical Research Coach, host Leanne Woehlke sits down with trailblazer Nasha Fitter—tech entrepreneur, rare disease advocate, and co-founder of both the FOXG1 Research Foundation and Citizen Health.


    After Nasha’s daughter was diagnosed with FOXG1 syndrome, an ultra-rare neurological disorder, her world shifted. Instead of accepting the limitations of the current research landscape, she took action- building a foundation, galvanizing the scientific community, and redefining what’s possible for families facing rare disease.


    What began as a grassroots foundation now drives innovative drug development, redefines data collection, and challenges the status quo in drug development.


    In this conversation, Nasha shares:

    • How a small, determined parent community raised $10M and launched a gene therapy program
    • Why traditional research models fail rare disease patients—and how to fix them
    • The power of patient-owned data and how platforms like Citizen Health are transforming access and insights
    • How to build empathy for families navigating special needs
    • What pharma gets wrong (and right) in working with advocacy groups
    • Her vision for a precision medicine future—starting with ultra-rare

    This is a story about courage, creativity, and a more inclusive, patient-driven future of medicine. Nasha’s bold vision and action oriented approach will leave you inspired and hopeful.


    To Find Out More:

    Nasha Fitter

    https://www.linkedin.com/in/nashafitter/

    FOXG1 Research Foundation:

    https://www.foxg1research.org/

    Citizen Health:

    https://www.citizen.health/




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    44 min
  • Hope, Loss and Legacy: Katie Diaz on Family, ALS and the Power of Purpose
    May 15 2025

    In this heartfelt episode, we sit down with Katie Diaz, Managing Partner of the Dan Diaz Biotech Breakfast Club. Katie shares the deeply personal story of her father, Dan Diaz, whose ALS diagnosis changed the course of her life- and inspired her to continue the work he started.


    Together we explore the importance of empathy, the emotional layers of navigating a rare disease and how Katie transformed grief into advocacy, mission and action.


    Enjoy!


    To Learn More:

    Katherine (Diaz) Harakel

    The Dan Diaz Biotech Breakfast Club:

    https://thedandiazbiotechbreakfastclub.godaddysites.com/



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    25 min

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