Medical Lead

Netanya, Israel · Full-time · Experienced

About The Position


  • Clinical Expertise: Serve as a primary medical resource within the company, providing clinical insights and expertise to inform product development decisions.
  • Medical Oversight: Provide medical oversight throughout the product development lifecycle, from concept ideation to regulatory approval and post-market surveillance.
  • Clinical strategy: Involve in the clinical strategy discussions and decisions for our AI clinical product, aligning with the company's overall vision and objectives.
  • Clinical Validation: Design and oversee clinical validation studies to demonstrate efficacy and utility of our product, collaborating with external clinical partners as needed.
  • Cross-functional Collaboration: Collaborate closely with interdisciplinary teams, including data science, engineering, product management, and regulatory affairs, to integrate medical considerations into product development
  • Hands-On clinical tasks: Lead and execute hands-on clinical tasks including mapping, clinical requirements definition, training sessions, and more
  • Customer-Facing responsibilities: Support sales and customer success through active participation in clinical discussions, assist in the implementation plans and executions


  • Medical degree (MD or equivalent)
  • At least 3 years of acute inpatient clinical experience, with a deep understanding of clinical workflows and challenges.
  • Prior experience in medical affairs, clinical development, or regulatory affairs within the healthcare industry
  • Prior experience in hospital clinical protocol development, Safety and quality projects, patient flow management, or clinical process implementation.
  • Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and external stakeholders
  • Willing to travel as needed.
  • Passion for innovation and improving healthcare outcomes through technology

Extra Points for

  • Two years of experience working in a US hospital environment
  • Extensive familiarity with regulatory mandates governing medical devices and software, particularly FDA regulations such as 510(k) and De Novo processes


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