• Shape the clinical product roadmap • You'll be the primary clinical voice in our product process, working closely with the Chief Delivery Officer as well as the Chief Technology Officer and reporting directly to the CEO. • You’ll ensure all our features, workflows and design decisions are grounded in clinical reality. • Translate frontline clinical experience into clear, evidence-based product requirements • Own the product roadmap, prioritising initiatives based on patient safety impact, clinical adoption, and commercial opportunity • Review feature specifications and user stories through a clinical governance lens before they enter development • Identify gaps in our current offering that represent genuine unmet clinical need and make the case for addressing them • Drive clinical adoption and customer success • Partner with our Delivery teams during implementations to ensure clinical workflows are configured correctly from day one • Support the development of Alertive communities, facilitating the sharing of best practice frameworks and SOPs • Work closely with customers to ensure they realise the full benefit of Alertive • Gather structured clinical feedback from live trusts and feed it back into the product cycle • Act as a point of escalation for complex clinical queries from our customer base • Lead on clinical safety and governance • Act as primary point of contact for our clinical safety consultancy and working alongside engineering to ensure risk is understood and managed appropriately. • Act as the internal expert on clinical workflow, escalation pathways, and safe messaging practice • Engage with clinical safety incidents and near-misses, translating learnings into product improvements • Support the sales and commercial team in high-value clinical conversations with medical directors, CNIOs, chief nurses, and clinical governance leads • Present at NHS conferences, clinical networks, and industry events as a credible advocate for Alertive's approach • Build and maintain relationships with clinical champions across our customer base • Contribute to case studies, white papers, and clinical content that builds Alertive's evidence base and market credibility • Contribute to strategic decisions, commercial conversations and the wider direction of the business, with your clinical perspective shaping how we think across the company.

• Provide remote leadership, mentorship, and supervision for Clinical Supervisors (Pod Leaders) • Support the client experience from intake through ongoing treatment across assigned centers • Conduct and review Functional Behavior Assessments (FBAs) • Ensure clinical excellence through quality assurance reviews, data analysis, and treatment oversight • Monitor treatment planning, progress monitoring, and program integrity • Maintain 30 billable hours per week providing QA oversight and clinical support to BCBAs without carrying a direct client caseload • Support performance management, coaching, and professional development of BCBAs and Program Supervisors • Partner with Operations leadership to strategically manage caseload distribution and staffing needs • Contribute to organizational growth initiatives, clinical standardization, and expansion into new markets • Foster collaboration and consistency across multiple centers through virtual leadership and communication

• Oversee protocol adherence to ensure clinical operations comply with current protocol, evidence-based medicine standards and applicable state and federal guidelines. • Enter into and maintain written Collaborative Practice Agreements/Supervisory Agreements as required by state law with each Nurse Practitioner (NP) or Physician Assistant (PA-C) employed by Ageless Men’s Health in our Pennsylvania locations as required. • Be generally available by telecommunications during clinic hours for consultation with NPs and PAs. • Conduct chart review as required under Pennsylvania Board of Medicine regulations. • Review and co-sign charts as required by individual agreements and Pennsylvania regulatory standards. • Ensure clinic operations comply with PA state medical practice laws, Board of Medicine regulations, and DEA requirements. • Maintain active Pennsylvania DEA registration to support lawful oversight of controlled substance prescribing, including testosterone and related medications. • Serve as a resource for clinical questions from NPs and PAs; provide timely consultations via phone, video, or messaging platforms.

Role Description This is the kind of role patent professionals talk about for the rest of their careers. You won’t inherit a slow-moving legal department buried under layers of review. You’ll help build one of the most ambitious medical-device patent operations being assembled anywhere today. - Protect breakthrough inventions across hydrogen inhalation systems, biosensors, wearable health technologies, and future-facing wellness devices. - Operate with rare ownership: Your judgment, your signature, your prosecution strategy, your name on the filings. - Work alongside an AI-powered invention engine moving at extraordinary speed while still owning the human expertise that matters most. - Help reshape the future of how medical-device innovation moves from concept to protected intellectual property. - This is not a maintenance role; it is a chance to help set a new standard for modern patent prosecution. Your next 5 minutes could land you in our top 5% shortlist — click Apply to start your application (a short, simple step to put you in the running). Registered USPTO Patent Agent – Medical Devices Domain ROLE SNAPSHOT — - Location/Schedule: Remote, Full-Time - Purpose: Own end-to-end prosecution for advanced medical-device and health-technology inventions within a high-speed AI-powered patent operation. Qualifications - Active USPTO Patent Bar registration in good standing. - Minimum 4 years of patent prosecution experience post-registration. - Minimum 50 patent applications drafted, prosecuted, or substantively responded to in medical-device, consumer-electronics, or sensor-hardware domains. - Strong engineering background: BSME, BSEE, BSBME, or equivalent; MS preferred. - Demonstrated expertise with §112(f) means-plus-function claim drafting and structural-support strategies. - Ability to independently sign and prosecute filings without attorney supervision. - Comfort operating in AI-assisted patent drafting workflows. - Ability to work at high production speed while maintaining substantive quality. Requirements - Prior in-house medical-device IP experience. - Experience at a top-tier patent prosecution practice focused on medical devices. - Familiarity with FDA 510(k) and PMA regulatory pathways. - Experience with hydrogen inhalation devices, biosensors, wearable devices, photobiomodulation hardware, or EMF-protection technologies. - Hands-on experience with AI-driven drafting systems. Benefits - Opportunity to help build a next-generation AI-powered patent operation. - High ownership and direct impact on strategic IP development. - Exposure to cutting-edge health and wellness technologies. - Fast-moving, innovation-focused environment. - Small, highly specialized team structure with significant autonomy. - Medical, Dental, and Vision coverage. - Accident, Hospital Indemnity, and Critical Illness. - Employee Assistance Program (EAP). - Employer Paid Life and AD&D Insurance. - Optional Supplemental Life and AD&D Insurance. - Short- and Long-Term Disability Insurance. - Flexible Spending Accounts. - Health Spending Accounts. - Dayforce Wallet – get paid as you earn. - Employee Discount. - Retirement Planning (401k with matching contribution). - Pet Insurance. - Wellness Program Offerings. - Paid Time Off, accrued per pay period based on years of service, starting at 20 days annually. - 9 Paid Holidays per year, including 1 floating holiday. Company Description Mercola and its affiliates (“Mercola”) are proud to be an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race (including hairstyle and texture), color, religion or belief (or lack thereof) (including religious grooming and dress practices), sex, nationality, national or ethnic origin, civil status, age, citizenship status, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. If you need accommodation, please send an email to hr@mercola.com to let us know the nature of your request.