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Chief risk officer • louisville ky
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Octave-XLouisville, KY, USLocation :
San Francisco, CA (Remote is also a possibility)
Salary : 250-275K
About Company / Opportunity :
We are creating next-generation open-source medical technologies that can enable clinicians to diagnose and treat potentially 100s of diseases with a single platform. With this advancement comes the promise of treatment of debilitating diseases including cancer, mental disease, stroke, COVID / Long COVID and longevity treatments. We already have a trove of clinical data demonstrating the promise of our technology, and now we are the world's first open-source, open-patent, open-clinical-data, and open-safety-sharing company, centered on the new idea of the Silicon Hospital.
Responsibilities :
The Chief Medical Officer (CMO) will play a pivotal role as the Company's primary clinical leader, serving as the external face of its medical and clinical vision. The CMO will engage with key stakeholders, including customers, key opinion leaders (KOLs), partners, investors, research institutions, patient advocacy groups, and other strategic constituents. By understanding and addressing the needs of these stakeholders, the CMO will help develop actionable clinical research and business strategies, objectives, and plans that align with the Company's short- and long-term goals.
As the clinical strategist for a groundbreaking open-source medical device company, the CMO will guide the advancement of innovative products in low-intensity focused ultrasound (LIFU) therapeutics and near-infrared (NIR) diagnostic platforms, ensuring they meet the widest set of global clinical needs while adhering to the relevant international regulatory standards. This role combines visionary leadership with hands-on collaboration to drive innovation, accessibility, and impact in healthcare technology.
Key responsibilities
- Collaborate with research partners to design clinical trials to (i) validate the efficacy and safety of the Company's open source medical devices; and (ii) use the Company's medical devices in novel applications across a variety of indications.
- Collaborate with external partners to design research and commercialization programs that advance science and deliver breakthrough solutions to patients while creating value for partners, the Company, and the greater community.
- Foster relationships with principal investigators, clinical research organizations (CROs), regulatory bodies (FDA / EMA), and key stakeholders.
- Participate in business discussions on behalf of the Company as the key clinical and regulatory subject matter expert.
- Lead clinical efforts, ensuring scientific rigor in all Company-sponsored studies, publications, and presentations.
- Develop and execute training plans for clinicians and staff on proper device and platform use.
- Stay informed on industry advancements, ensuring the Company remains at the forefront of research and clinical development.
- Provide clinical and regulatory input to define product specifications to fit target indications and overall clinical and regulatory strategy.
- Gather and incorporate perspective from the end users (i.e. clinicians) into product strategy.
- Analyze data from the Company's products to determine quality and effectiveness.
Regulatory
Business Development
Required Skills & Experience
Preferred Skills
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