Clinical Specialist Remote Jobs in Wisconsin (US)
This page tracks remote clinical specialist openings that are location-eligible for Wisconsin.
This page tracks remote clinical specialist openings that are location-eligible for Wisconsin.
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23
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$39 - $195,000
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23 Jobs
14 Companies
Powering superior telehealth from end-to-end. #HealingAnywhere
• Serve as the clinical subject matter expert (SME) for product and project teams, providing guidance on clinical workflows, clinical knowledge, and best practices for clinical data • Design, build, test, and update clinical data assets that provide clinical decision support and drive clinical workflows, - ensuring their ongoing accuracy, completeness, and clinical validity over time • Translate clinical requirements into workflow and informatics/data specifications, and validate that delivered features reflect sound clinical reasoning • Analyze clinical data to identify gaps, inconsistencies, and opportunities for improvement, and apply findings to enhance decision support logic and workflow automation • Review technical specifications for clinical workflow applications to provide clinical informatics input - and provide support as SME and IC for product managers leading clinical application products • Maintain and curate mappings to standardized clinical and medical vocabularies, supporting interoperability and consistency across systems • Collaborate with clinical, product, and engineering stakeholders to ensure data-driven features are safe, usable, and clinically meaningful • Partner with clinical leadership to support guideline development, clinical content governance, and quality and product enhancements • Work closely with Quality and Clinical Training/Education teams to identify areas of improvement for clinical workflows across the organization; collaboratively design and implement solutions • Other duties as assigned
Founded in 2004 and led by CEO Steve Chapman, Natera is a company in the biotechnology market that offers genetic testing and diagnostics on a global scale. Ope
Role Description The Clinical Oncology Specialist (COS) is a high-impact, clinical sales role that leverages deep oncology, pathology, and molecular diagnostics expertise to drive the adoption and utilization of Natera’s advanced oncology portfolio. As a crucial clinical partner, the COS will navigate complex, large academic health systems to bridge the gap between medical oncology and surgical oncology, ensuring seamless integration of Natera's testing into patient care pathways. The COS acts as a strategic collaborator across territories, working cross-functionally with internal oncology team members—including women’s health, pharmaceutical sales teams, and medical affairs—to formulate and execute unified strategic accounts plans. This is accomplished through high-level clinical dialogue, targeted provider education, and the implementation of efficient workflow processes for appropriate patient identification. Primary Responsibilities - Navigate Academic & Clinical Ecosystems: - Establish a strong presence within large academic health systems, complex cancer centers, and community clinics. - Engage both medical oncologists and surgical oncologists to integrate Natera diagnostics into multidisciplinary tumor boards and clinical pathways. - Cross-Functional Collaboration: - Partner seamlessly with internal cross-functional oncology team members (including molecular sales specialists, women’s health, pharma sales, and medical affairs) to align strategy, share insights, and maximize market penetration within the territory. - Drive Clinical Adoption: - Execute targeted sales strategies and deliver approved clinical marketing messages to key opinion leaders (KOLs), physicians, and hospital stakeholders to influence test adoption and volume growth. - Market & Product Expertise: - Maintain a commanding knowledge of Natera’s products, services, and reimbursement landscape, as well as competitor offerings, molecular pathology trends, and personalized medicine advancements. - Account Workflow Optimization: - Identify logistical and clinical barriers to testing within institutions; implement streamlined processes for patient identification, sample acquisition, and result delivery. - Account Management & Retention: - Monitor, document, and report on existing business health, proactive competitive threats, and new market opportunities. - Act as a clinical concierge to escalate and swiftly resolve client issues. - Ethical Compliance: - Conduct all business, clinical discussions, and field interactions with the highest level of integrity, compliance, and transparency. Qualifications - Education & Experience: - Bachelor’s degree with at least 5 years of direct oncology experience OR an Associate degree with at least 7 years of direct oncology experience. - Market Knowledge: - Deep, pre-existing knowledge of the local oncology market, including key institutional networks and community oncology practices. - Clinical Acumen: - Robust understanding of oncology molecular diagnostics, next-generation sequencing (NGS), liquid biopsy, and the broader landscape of personalized medicine. Knowledge, Skills, and Abilities - Multidisciplinary Fluency: - Ability to confidently engage and speak the language of both medical and surgical oncology stakeholders, understanding their distinct clinical priorities. - Collaborative Spirit: - A proven track record of working effectively in highly cross-functional matrix environments, acting as a team player who lifts collective territory goals. - Communication Excellence: - Exceptional presentation, communication, and interpersonal skills, with the ability to translate complex molecular data into actionable clinical utility. - Strategic Self-Starter: - Autonomous, forward-thinking professional with strong business analysis skills and a keen grasp of healthcare business and reimbursement trends. Physical Demands & Work Environment - Duties are typically performed in a medical office or hospital setting. - This position requires the ability to use a computer keyboard, communicate over the telephone, and read printed material. - Duties may require working outside normal working hours (evenings and weekends) at times. - 50% travel required. Benefits - In addition to a base salary, we offer uncapped commission, a car allowance program, and Restricted Stock Units (RSUs). - The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications, and specific office location. - Remote USA: $195,000 — $225,000 USD. Company Description Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives. - The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers, and many other professionals from world-class institutions, who care deeply for our work and each other. - When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.
We pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.
• deliver best-in-class Clinical Education on Siemens CT Imaging systems and components • providing expert technical training that fosters customer excellence • prepare and gather necessary regulatory-approved documentation for end-user training • engage in effective and professional communication with internal and external stakeholders • conduct clinical training to educate staff on how to use Siemens equipment safely and effectively • complete regulatory and core process documents per policy guidelines • coordinate and facilitate training activities that result in excellent clinical outcomes
Powering superior telehealth from end-to-end. #HealingAnywhere
• Assist in the maintenance and optimization of clinical onboarding modules within the Learning Management System • Ensure training materials reflect current practices, workflows, and platform capabilities • Support provider readiness by monitoring metrics and feedback related to onboarding and training activities. • Monitor designated communication channels to identify, triage, or escalate clinical or technical onboarding issues • Maintain and update clinical documentation and training materials across verticals and clients • Translate clinical workflows, regulatory requirements, and platform updates into clear, user-friendly educational materials • Assist in the development of new training resources related to clinical initiatives, workflow enhancements, or product updates • Support knowledge base management • Support the Sr. Clinical Specialist (NP) in coordinating required and supplemental materials for client launch preparedness • Collaborate with cross-functional teams to ensure clinical readiness for go-live • Participate in regular Clinical Education team meetings to align on priorities, share insights, and address challenges • Collaborate cross-functionally with Clinical Operations and Quality teams to support training and implementation efforts • Contribute to the ongoing refinement of clinical onboarding, training programs, and launch workflows to improve scalability and effectiveness • Identify trends, gaps, or recurring issues in provider education and escalate recommendations • Support quality improvement initiatives related to clinical training and provider performance • Assist with additional duties as assigned
• Deliver compelling, clinically accurate product demonstrations to prospective customers in partnership with Sales Account Executives. • Support the sales cycle by addressing clinical workflows, use cases, and outcomes-related questions from clinicians and administrators. • Conduct clinical onboarding and training sessions (virtual and in-person) for new customers, tailored to specific clinical roles and workflows. • Develop and refine clinical training materials, best practices, and enablement resources in collaboration with Product, Customer Success, and Marketing. • Provide ongoing clinical guidance, workflow optimization recommendations, and product usage insights post-implementation. • Participate in customer check-ins, QBRs, and feedback loops to capture clinical insights and inform product improvements. • Act as the voice of the clinician internally, providing feedback to Product and Engineering teams on usability, workflow alignment, and feature needs. • Support internal enablement by training Sales, Customer Success, and other teams on clinical use cases and product updates. • Ensure all customer-facing activities align with regulatory, compliance, and quality requirements applicable to medical devices and SaMD products. • Maintain current knowledge of clinical best practices, industry standards, and relevant healthcare regulations.
Powering superior telehealth from end-to-end. #HealingAnywhere
• Execute high-volume, structured audits of provider charts to ensure protocol alignment and documentation accuracy. • Assist Quality RNs in "deep-dive" investigations to identify systemic gaps and process failures. • Monitor and maintain the database for provider quality trainings, ensuring 100% compliance during mass hiring cycles. • Disseminate approved quality messaging and educational updates to the provider population with professional tact. • Work across the organization to flag issues in the "intake-to-implementation" pipeline, preventing errors before they reach the clinical stage. • Jump in to support any team member or department project as organizational needs shift—we tackle every problem as a unified front.
As an employer, Abbott is interested in candidates who are passionate about creating healthy solutions and making a difference in the world. Abbott offers compe
Role Description This position is a field-based position based in Little Rock, AR in the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias or irregular heartbeats. Under general direction, the CRM Product Support Specialist provides comprehensive engineering, sales, educational, and technical support. This role responds to field inquiries from physicians, healthcare professionals, patients, and field sales staff regarding CRM (Cardiac Rhythm Management) products. Key Responsibilities - Clinical Interface: Acts as a senior clinical interface between the medical community and the business. - Relationship Building: Demonstrates the ability to build and sustain credible business relationships with customers and share product expertise accordingly. - Comprehensive Support: Provides engineering, sales, education, and clinical support in response to field inquiries on an as-needed basis. Demonstrates a thorough command of all CRM products, related product and technical knowledge, trends, and players while providing regional case coverage. - Training and Education: Develops, leads, and/or facilitates training sessions and other programs on CRM products for healthcare professionals. - Sales Support: Provides additional back-up support to Cardiac Rhythm Team in the following areas: - Sales support - Regional training seminars - Clinical studies/data collection - Trouble Shooting - New product in-service training to physicians, nurses and sales representatives - Mentors and provides leadership for less experienced Clinical Specialists. - Continuously develops engineering, sales and technical skills relative to the overall Arrhythmia Management strategy, including learning opportunities via Sr. Sales personnel and management. Qualifications - Bachelor’s degree in Bio-Medical Engineering, related field or equivalent healthcare experience. - 6+ years of related experience or a program certification from an accredited cardiac training program. - Must have IBHRE certification in CRM products for this role. - Demonstrated knowledge of cardiology, electro-physiology, or cardiac electro-physiology procedures. - Familiarity with cath lab and operating room procedures and protocol. - Demonstrate advanced knowledge of cardiac pacing systems. - Must apply engineering skills and abilities to interpret and solve complex clinical problems. - Must possess strong written and verbal communication skills, along with excellent interpersonal, presentation, analytical, and organizational abilities. - Must be detail-oriented and capable of working independently. - Must be able to collaborate effectively with engineers, technical specialists, vendors, and customers to achieve assigned goals. - Must have extensive personal computer skills, including experience with Microsoft Office or equivalent software. Requirements - Must be capable of managing multiple assignments simultaneously and efficiently. Benefits - Career development with an international company where you can grow the career you dream of. - Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. - An excellent retirement savings plan with a high employer contribution. - Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. - A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune. - A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
We pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.
• Deliver best-in-class Clinical Education on Siemens CT Imaging systems and components • Provide expert technical training that fosters customer excellence • Work with modality team to develop clinically relevant knowledge and expertise • Prepare regulatory-approved documentation for end-user training • Engage in effective communication with stakeholders • Conduct clinical training for staff on Siemens equipment • Complete regulatory and core process documents as per policy guidelines • Coordinate training activities resulting in excellent clinical outcomes
Role Description The Appeals team oversees all operational and clinical aspects of the appeals process, including intake, case processing, clinical determinations, notifications, and compliance with regulatory and accreditation standards. The Appeal Clinical Specialist is responsible for independently conducting clinical reviews as part of the appeals process. This role includes: - Evaluating medical records - Applying clinical criteria and guidelines - Making determinations regarding benefit coverage - Ensuring all appeal reviews are completed accurately and in a timely manner - Supporting the integrity and quality of the appeals process This position focuses on initiating, supporting, and maintaining cost-effective, rational drug, and disease therapy. Essential Duties and Responsibilities - Provide appeal clinical support services to client plan(s) contracting for appeal clinical services, including clinical review, analysis, recommendation, decision, and documentation of appeal requests. - Review medication request guidelines for clinical appropriateness and operational efficiency. - Provide drug information support and research clinical literature documentation to support prior authorization decisions. - Coordinate and assist in the preparation of utilization and compliance reporting for client plans. - Coordinate and assist with projects associated with appeal program development, implementation, and internal and external communications. - Provide feedback to Prior Authorization team and Appeals and Grievances Coordinators regarding the processing of appeal cases referred for clinical review. Qualifications - PharmD and 3+ years’ experience or equivalent combination of education and experience, and 1 year of SME in respective areas. - Strong computer skills with Microsoft Office and Microsoft Outlook; good working familiarity with databases and internet searches. - Current, unrestricted Registered Pharmacist license in good standing in any state within the United States. - Excellent working knowledge of all types of pharmacy services with an emphasis on the managed health care environment. - Expertise in clinical application of pharmacy practice. Requirements - Ability to solve practical problems and deal with a variety of concrete variables. - Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. - Ability to work with mathematical concepts such as probability and statistical inference. - Ability to write reports, business correspondence, and procedure manuals. - Ability to effectively present information in one-on-one and small group situations. - Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Competencies - Composure - Decision Quality - Organizational Agility - Problem Solving - Customer Focus - Drive for Results - Peer Relations - Time Management - Dealing with Ambiguity - Learning on the Fly - Political Savvy Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job: - Regularly required to sit, talk, or hear. - Regularly required to stand, walk, use hands to finger, handle, or feel and reach with hands and arms. - Must occasionally lift and/or move up to 25 pounds. - Ability to maintain clear near visual acuity to accurately read fine print and view computer screens. Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job: - Regularly exposed to moving mechanical parts, high precarious places, fumes, or airborne particles. - Noise level in the work environment is usually moderate. Work Location This position works on-site at the San Diego Headquarters or other company location (or from a remote location with management approval based on business requirements). Working Hours This is a full-time non-exempt position requiring the ability to work overtime from time to time. The typical working hours are Monday through Friday from 8:00am to 5:00pm. Travel This position requires no travel; however, attendance may be required at various local conferences and meetings. Benefits - Medical / Dental / Vision / Wellness Programs - Paid Time Off / Company Paid Holidays - Incentive Compensation - 401K with Company match - Life and Disability Insurance - Tuition Reimbursement - Employee Referral Bonus Company Description MedImpact, is a privately-held pharmacy benefit manager (PBM) headquartered in San Diego, California. Our solutions and services positively influence healthcare outcomes and expenditures, improving the position of our clients in the market.
Stanford Health Care is a division of Stanford Medicine—a segment of Stanford University. As an employer, Stanford Health Care has offered job opportunities t
Role Description The Senior Denial Specialist is responsible for the timely and accurate resolution of denied claims in accordance with current contracts, federal regulations, and SHC policies. The Senior Denial Specialist serves as a subject matter expert and has extensive experience in denial resolution and recovery. Responsibilities may include high dollar and complex denial review and resolution, complex appeals, and serves as a mentor for new employees. The Senior Denial Specialist position is an expert-level position with a proven track record in hospital and physician denial resolution, and has an extensive knowledge of reimbursement requirements of all types of healthcare payers. A Senior Denial Specialist will act as a key resource for management in problem-solving difficult issues, analyzing complex accounts, and assisting with training needs. What you will do - Work a broad range of denied claims taking necessary actions to recover and resolve in accordance with contracts, federal regulations, and SHC policies. - Conduct root-cause analysis on denied claims to identify opportunities for mitigation and escalation. - Monitor high dollar and complex denial work queues, follow up on denied or underpaid appealed claims, and track appeal deadlines. - Collaborate with appropriate leadership and stakeholders to escalate trends and issues related to internal processes or external payer behavior. - Maintain accurate documentation in Epic and related systems; ensure compliance with privacy and regulatory requirements. - Support special projects related to high dollar or complex denials as assigned by management. - Provide cross-functional communication with Revenue Cycle teammates, payers, and patients as needed to resolve denial issues professionally. Qualifications - High School diploma or GED equivalent. - Five (5) years of progressively responsible and directly related work experience in healthcare revenue cycle, with a minimum of three (3) years of direct experience in denial management. Requirements - Working knowledge of government and non-government payer requirements, reimbursement rules, laws, and regulations that govern billing/collection activities. - Working knowledge of Epic Hospital and/or Professional Billing; proficiency in Epic reporting preferred. - Working knowledge of medical terminology, CPT-4, ICD-9/ICD-10, HCPCS, and modifiers, and how these items drive reimbursement. - Analytical and problem-solving skills, with good judgment, attention to detail, and thorough follow-through. - Excellent verbal and written communication skills; ability to present complex data clearly to stakeholders. Licenses and Certifications - CPC - Certified Professional Coder required Upon Hire or - CRCR - Certified Revenue Cycle Representative required Upon Hire. Company Description Stanford Health Care sets a high standard for delivering value and an exceptional experience for our patients and families. Candidates for employment and existing employees must adopt and execute C-I-CARE standards for all of patients, families and towards each other. C-I-CARE is the foundation of Stanford’s patient-experience and represents a framework for patient-centered interactions. Simply put, we do what it takes to enable and empower patients and families to focus on health, healing and recovery. - Know Me: Anticipate my needs and status to deliver effective care. - Show Me the Way: Guide and prompt my actions to arrive at better outcomes and better health. - Coordinate for Me: Own the complexity of my care through coordination.
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