Medical Lead
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
Requirements
- 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