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: 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.
This position is open to all candidates.