• Provide medical, scientific, and clinical expertise for MCED strategy, clinical protocols, regulatory submissions, and study design. • Serve as the principal internal medical authority for MCED programs, ensuring scientific rigor and alignment with corporate objectives. • Interpret and communicate clinical and analytical performance data, including safety, efficacy, and real-world evidence. • Oversee development of scientific publications, abstracts, peer-reviewed manuscripts, and presentations. • Partner cross-functionally with Regulatory, Clinical Operations, Biostatistics, R&D, Product, Market Access, and Commercial teams to ensure seamless program execution and clinical relevance. • Engage and cultivate relationships with external experts, investigators, clinical partners, advocacy groups, and regulatory agencies. • Act as the lead internal physician representing the clinical user experience and real-world clinical workflows for Caris’ MCED products. • Represent Caris at national and international scientific meetings, advisory boards, and industry forums. • Monitor emerging trends in oncology, early detection, liquid biopsy, genomics, biomarkers, and relevant clinical practice guidelines to inform strategy and innovation.