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YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_27f4de0f-b9b"},"title":"Regional Medical Director","description":"<p>You will be the second Medical Lead on a interdisciplinary population health team, serving as a primary clinical supervisor and educator for Waymark&#39;s Midwest and West Coast markets. Over the next 18 months, you will help clinically oversee our AI-augmented care navigation platform for Medicaid populations,reviewing and triaging patient escalations in real time, alternating monthly care delivery education sessions with your co-Medical Lead, and conducting weekly multidisciplinary rounds across your regional care teams. You will also share rotating on-call coverage for urgent after-hours escalations (these are rare) and serve as Waymark&#39;s clinical face to the health system and health plan clinical leadership in your markets.</p>\n<p>Key Responsibilities:</p>\n<ul>\n<li>Conduct weekly multidisciplinary rounds with Midwest and West Coast care teams, reviewing patient goals, complex medical and social situations, and providing clinical oversight and outcome-improvement strategies.</li>\n</ul>\n<ul>\n<li>Serve as the designated reviewer and triaging physician for COMPASS patient escalations as they enter the queue, applying clinical judgment to prioritize and direct AI-flagged cases to appropriate next steps.</li>\n</ul>\n<ul>\n<li>Alternate monthly care delivery education sessions with co-Medical Lead, developing and facilitating case-based learning (e.g., SUD management, integrated behavioral health, heart failure, steroid-induced hyperglycemia, functional seizures) for CHWs, care coordinators, pharmacists, and therapists.</li>\n</ul>\n<ul>\n<li>Provide asynchronous and synchronous clinical supervision to licensed therapists (LCSW/LMFT) and pharmacist teams, including time-sensitive escalations such as acutely suicidal or medically unstable patients.</li>\n</ul>\n<ul>\n<li>Rotate on-call coverage with co-Medical Lead for rare after-hours urgent clinical escalations and questions from field teams.</li>\n</ul>\n<ul>\n<li>Serve as the clinical dyad partner for regional operations leads, supporting market performance against quality, HEDIS, and outcomes OKRs.</li>\n</ul>\n<ul>\n<li>Represent Waymark at regional and national meetings with health system and health plan physician leadership, including presentations to MCO and FQHC Chief Medical Officers on Waymark&#39;s care model and COMPASS platform.</li>\n</ul>\n<ul>\n<li>Maintain current knowledge of clinical best practices across primary care, integrated behavioral health, street medicine, and population health, and contribute to quarterly clinical guideline reviews.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_27f4de0f-b9b","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Waymark","sameAs":"https://waymark.com","logo":"https://logos.yubhub.co/waymark.com.png"},"x-apply-url":"https://job-boards.greenhouse.io/waymark/jobs/4327699005","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$207,000 – $267,000","x-skills-required":["Medical degree (MD/DO)","Active medical license in any U.S. state","Board certification in family medicine, internal medicine, med-peds, or emergency medicine","Experience in safety-net, FQHC, street medicine, or overnight/urgent triage settings","Competency in integrated behavioral health, substance use/addiction medicine, and care of people experiencing homelessness or housing instability"],"x-skills-preferred":["Experience in Medicaid managed care, value-based care contracting, or population health programs","Familiarity with SMS-based or asynchronous digital health platforms and clinical oversight workflows","Experience presenting clinical data or care model performance to external physician or executive audiences","Background in clinical quality improvement, HEDIS measurement, or care model design","2+ years in a health tech company or startup environment"],"datePosted":"2026-04-24T17:08:51.357Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"US - 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COPD Biologics","description":"<p>The US Medical Director – COPD Biologics provides US-focused medical leadership for all phases of Chronic Obstructive Pulmonary Disease (COPD). The role is an integral part of the US Core Medical Team (CMT) and serves as the primary US medical point of accountability for scientific strategy, evidence generation, and external engagement.</p>\n<p>This role is ideally suited for a physician or pharmacist with deep expertise in pulmonary medicine and experience across late-stage development, launch readiness, and post-approval medical excellence. The Medical Director ensures US medical strategy is aligned with global direction while remaining responsive to the healthcare and clinical landscape within the United States.</p>\n<p>At AstraZeneca, teams work across global boundaries to make an impact and find answers to complex challenges. This role sits at the heart of that mission, combining scientific depth with strategic leadership to advance care in chronic respiratory disease.</p>\n<p>This position completes the medical strategy and carries out the execution for a novel Interleukin-33 targeting monoclonal antibody, crafting both product and disease area direction across the full lifecycle.</p>\n<p>Reporting directly to the US Medical Head, COPD Biologics, this leader will guide a high-performing team, drive launches, and influence how evidence, access, and clinical practice come together to transform outcomes for patients living with COPD and severe lower respiratory tract disease.</p>\n<p>Accountabilities:</p>\n<p>US Medical Strategy &amp; Asset Leadership - Serve as the US medical lead for COPD Biologics, accountable for development and execution of the US Brand Medical Plan across pre and post-approval stages.</p>\n<p>Provide strategic medical input to US brand and launch strategy, ensuring alignment of scientific priorities with patient and clinical needs.</p>\n<p>Translate complex biology, clinical data, and disease state-insights into actionable US medical strategies.</p>\n<p>Pre-Approval Medical Affairs Responsibilities - Lead US medical strategy for late-stage clinical development, including:</p>\n<p>US input into Phase 3/3b study design</p>\n<p>Endpoint relevance to US clinical practice</p>\n<p>Subpopulation and biomarker strategy</p>\n<p>Support US regulatory readiness through medical review, scientific positioning, and collaboration with regulatory and global partners.</p>\n<p>Develop and implement pre-approval external scientific engagement strategy consistent with regulations, including:</p>\n<p>Scientific exchange on disease biology and unmet need</p>\n<p>Advisory boards focused on clinical trial interpretation and future treatment paradigms</p>\n<p>Contribute to launch readiness planning, including:</p>\n<p>Medical education strategy</p>\n<p>Scientific platform development</p>\n<p>Medical training for Field Medical teams</p>\n<p>Partner with evidence, payer, and outcomes teams to define early value evidence strategy relevant to the US healthcare environment.</p>\n<p>Post-Approval Medical Affairs Responsibilities - Lead ongoing post-approval medical strategy to support appropriate scientific exchange and optimize patient care.</p>\n<p>Lead all aspects of Phase 4 and lifecycle management strategy, including real-world-evidence (RWE) and effectiveness studies relevant to US clinicians and payers.</p>\n<p>Provide medical leadership for:</p>\n<p>US publication strategy and congress planning</p>\n<p>Medical review of promotional and non-promotional materials</p>\n<p>Scientific response strategy and data dissemination</p>\n<p>Serve as a medical spokesperson for the US brand as appropriate, supporting external scientific discussions and media inquiries.</p>\n<p>Maintain accountability for the evolving US product scientific narrative, incorporating new data, guidelines, and real-world insights.</p>\n<p>External Engagement &amp; Scientific Exchange (US Focused) - Design and implement a comprehensive US external engagement plan, including:</p>\n<p>Key Opinion Leaders (KOLs)</p>\n<p>Academic institutions</p>\n<p>Integrated delivery networks and hospital systems</p>\n<p>Professional societies</p>\n<p>Lead planning and participation in national and regional US medical advisory boards.</p>\n<p>Ensure high-quality, compliant scientific exchange that advances understanding of COPD pathophysiology.</p>\n<p>Evidence Generation &amp; Medical Governance - Collaborate with medical evidence and payer teams to design and implement:</p>\n<p>Clinical effectiveness studies</p>\n<p>RWE and health outcomes research</p>\n<p>Provide medical review and governance for Externally Sponsored Research (ESR) proposals.</p>\n<p>Provide medical input into product safety strategy in collaboration with Patient Safety colleagues.</p>\n<p>Ensure compliance with all US regulatory requirements, OPDP standards, PhRMA Code, and AstraZeneca policies.</p>\n<p>Internal Collaboration &amp; Capability Building - Provide clinical education and scientific training for:</p>\n<p>US Field Medical organization</p>\n<p>Cross-functional-partners (commercial, market access, HEOR)</p>\n<p>Act as a trusted US medical advisor to internal team members on COPD disease strategy and emerging science.</p>\n<p>Maintain strong collaboration with global medical and clinical teams, ensuring seamless alignment while representing US medical needs.</p>\n<p>Minimum Requirements - Doctoral degree (MD, PhD, MBBS or PharmD) or equivalent education</p>\n<p>3+ years of demonstrated experience or strong expertise in Pulmonary Medicine, respiratory pharmacology, or immune-mediated-disease.</p>\n<p>Experience in late-phase clinical development and/or post-approval medical affairs.</p>\n<p>Well-developed comprehension of the US regulatory environment, including FDA and 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Executive Medical Director, Specialty and Pipeline to oversee the development and execution of high-quality medical strategy for our pipeline portfolio.</p>\n<p>As a critical member of the US Medical Affairs team, you will be responsible for providing scientific leadership, external engagement, and cross-functional influence to advance evidence generation, medical education, and development of medical affairs strategy to support commercialization strategic plans of the portfolio.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Overseeing US medical affairs strategy and contributions into the Bayer pipeline portfolio in collaboration with medical directors and in alignment with the VP of Specialty and Pipeline TA.</li>\n<li>Providing input, appropriate to the Phase of development of a product to ensure US perspective and needs are incorporated into development strategy.</li>\n<li>Active participation and effective collaboration with global teams to assure the efficient and expedient conduct of clinical development programs, aligning them with strategic priorities that support appropriate US direction of the Life Cycle Management strategy.</li>\n<li>Working collaboratively with US New Product Commercialization, Market Access and US regulatory teams to provide expert medical input into strategic plans.</li>\n<li>Serving as a member of Product Team and/or Clinical Strategy Team leadership of multiple assets in different therapeutic areas.</li>\n<li>Supporting development and execution of the US medical strategy, offering critical inputs during design and throughout the end-to-end execution of programs, in alignment with senior medical leadership.</li>\n<li>Collaborating cross-functionally with Global Evidence Generation, Clinical Development, Regulatory, Commercial and other medical affairs partners to develop and implement the Integrated Evidence Plans to improve the value proposition for the portfolio.</li>\n<li>Contributing to publication planning, data interpretation, and scientific dissemination in the US.</li>\n<li>Providing medical scientific input for brand and program documents, including integrated disease area plans, medical information documents, drug safety reporting documents, etc, while ensuring design and execution of all medical activities are according to internal and external compliance guidelines.</li>\n<li>Monitoring and understanding implications of evolving competitor landscape to inform medical strategy.</li>\n<li>Supporting completion of annual New Drug Application (NDA) reports for respective brands through evaluation of clinical data and literature and provide US Medical Affairs input in the preparation of key medical documents for INDs and NDAs.</li>\n</ul>\n<p>Additionally, you will:</p>\n<ul>\n<li>Develop and guide local Thought Leader (TL) engagement strategy, together with cross-functional partners.</li>\n<li>Serve as the US medical expert engaging thought leaders, academic institutions, medical societies, and patient advocacy groups to advance scientific leadership and collaboration.</li>\n<li>Lead and support advisory boards, including agenda development, faculty engagement and synthesis of insights to help inform medical strategy.</li>\n<li>Represent US Medical Affairs at major congresses, symposia and scientific forums.</li>\n</ul>\n<p>To be successful in this role, you will need:</p>\n<ul>\n<li>An M.D. or D.O. degree.</li>\n<li>Agility and ability to flex into different therapeutic areas.</li>\n<li>Clinically relevant work experience or independent research experience or equivalent or experience in a pharmaceutical related industry.</li>\n<li>Experience working in or deep understanding of in-hospital consideration in US healthcare delivery.</li>\n<li>Deep understanding of clinical trial design, analysis and interpretation as well as the principles of observational studies and health economics/ outcomes research.</li>\n<li>Robust understanding of regulatory and market access considerations and triangulating those to implications on clinical trial design and clinical care delivery.</li>\n<li>Proven ability for strategic planning along with operations skill and experience related to clinical research involving both single and multiple centers.</li>\n<li>Strong ability to quickly build meaningful and trusting relationships, both internally and externally to the organization.</li>\n<li>Understanding of the drug development process over different stages.</li>\n<li>Strong ability to connect and collaborate across different functions and background, both internally and externally to the organization.</li>\n<li>Innate ability to lead others without formal authority, with demonstrated experience guiding teams from design to implementation of strategic initiatives.</li>\n<li>Excellent communication skills, both verbal and in written.</li>\n<li>Willingness and ability to travel as business dictates, both for internal and external functions.</li>\n</ul>\n<p>Preferred 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dictates, both for internal and external functions, Board certification or board eligibility in cardiovascular, neurology, critical care medicine, 7 years work experience in the pharmaceutical sector in Medical Affairs, Clinical Development or related positions, Experience in the field of medical support of a product portfolio across multiple therapeutic areas, Experience in leading and participating in teams across cultures and geographies, prior experience in global medical launch planning activities","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":248000,"maxValue":372000,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_e402b6af-005"},"title":"Physician","description":"<p>Join knownwell, a company changing the way obesity care is delivered. As a Physician, you will work alongside a team to provide comprehensive medical care, focusing on the diagnosis, treatment, and prevention of obesity and obesity-related conditions. This position offers an opportunity to make a significant impact on patients&#39; lives by helping them improve their overall health.</p>\n<p>Responsibilities:\nProvide compassionate, evidence-based medical care to patients with obesity and obesity-related metabolic conditions.\nDeliver longitudinal primary care services to a panel of patients across both in-clinic and virtual care settings.\nDevelop and implement individualized, patient-centered treatment plans integrating pharmacotherapy, lifestyle medicine, nutrition, and behavioral health approaches.\nCollaborate with advanced practice clinicians, registered dietitians, and behavioral health providers to support a team-based model of care.\nPartner with the National Medical Director and clinical leadership to uphold and advance clinical quality standards and care protocols.\nContribute to a weight-inclusive, non-stigmatizing care culture consistent with knownwell&#39;s mission and values.\nParticipate in ongoing clinical education, quality improvement initiatives, and team meetings.</p>\n<p>Requirements:\nMD or DO degree with successful completion of residency training in Family Medicine, Internal Medicine, or a related primary care specialty.\nActive, unrestricted medical license in the state of Georgia (or ability to obtain prior to start).\nDEA registration.\nStrong interest in and commitment to obesity medicine and metabolic health.\nExperience managing patients with chronic cardiometabolic conditions in a primary care or outpatient setting.\nDedication to weight-inclusive, evidence-based, and patient-centered care.</p>\n<p>Preferred qualifications include board certification or active candidacy in Obesity Medicine (ABOM), experience with anti-obesity medications, comfort working in hybrid care models, and experience with or interest in APC collaboration and supervision.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_e402b6af-005","directApply":true,"hiringOrganization":{"@type":"Organization","name":"knownwell, Inc.","sameAs":"https://www.knownwell.com/","logo":"https://logos.yubhub.co/knownwell.com.png"},"x-apply-url":"https://jobs.lever.co/knownwell/73964a00-28ae-41fc-b8db-b5c940bbafb8","x-work-arrangement":"hybrid","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["MD or DO degree","Residency training in Family Medicine, Internal Medicine, or a related primary care specialty","Active, unrestricted medical license in the state of Georgia","DEA registration","Strong interest in and commitment to obesity medicine and metabolic health","Experience managing patients with chronic cardiometabolic conditions"],"x-skills-preferred":["Board certification or active candidacy in Obesity Medicine (ABOM)","Experience with anti-obesity medications","Comfort working in hybrid care models","Experience with or interest in APC collaboration and supervision"],"datePosted":"2026-04-17T12:40:11.751Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Atlanta"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"MD or DO degree, Residency training in Family Medicine, Internal Medicine, or a related primary care specialty, Active, unrestricted medical license in the state of Georgia, DEA registration, Strong interest in and commitment to obesity medicine and metabolic health, Experience managing patients with chronic cardiometabolic conditions, Board certification or active candidacy in Obesity Medicine (ABOM), Experience with anti-obesity medications, Comfort working in hybrid care models, Experience with or interest in APC collaboration and supervision"}]}