• Build Scalable Clinical Infrastructure • Develop and operationalize condition-specific SOPs (ADHD, anxiety, depression, PTSD, medical weight loss) • Establish structured prescribing frameworks, titration pathways, and monitoring standards • Define inclusion/exclusion criteria and clinical guardrails • Reduce variability across providers and service lines • Own Quality & Provider Performance • Design and lead structured chart audit programs and peer review systems • Monitor prescribing patterns and documentation quality • Define measurable clinical KPIs and maintain performance dashboards • Lead remediation processes and performance improvement plans when needed • Escalate complex or high-risk cases to the CMO • Strengthen Documentation & Compliance Systems • Standardize EMR templates and intake/follow-up workflows • Embed structured documentation fields to improve defensibility and audit readiness • Operationalize stimulant safeguards and GLP-1 safety monitoring protocols • Establish adverse event review and escalation pathways • Partner Cross-Functionally • Collaborate with Product & Engineering to translate SOPs into scalable workflows • Review AI-assisted documentation tools and establish guardrails • Validate clinical accuracy of patient-facing and marketing materials • Ensure operational alignment between growth initiatives and clinical safety • Clinical Practice (10–20%) • Maintain a limited patient panel within core service lines • Model SOP adherence and documentation standards • Identify workflow friction and system improvement opportunities