Clinical Specialist Remote Jobs in Minnesota (US)
This page tracks remote clinical specialist openings that are location-eligible for Minnesota.
This page tracks remote clinical specialist openings that are location-eligible for Minnesota.
Open jobs
26
Hiring companies this week
7
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$74,350 - $195,000
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26 Jobs
15 Companies
• Build and maintain Leap's outcomes framework across adherence, safety, patient-reported outcomes, and disease-specific clinical measures. • Define metric definitions, denominator and numerator logic, inclusion criteria, calculation methods, and validity standards. • Align outcomes methodologies with recognized specialty pharmacy, home infusion, and quality measurement standards where appropriate (e.g., NHIA quality measures and other industry benchmarks). • Maintain clear documentation of metric definitions, methodology updates, and the rationale for changes over time. • Define and stand up Leap's safety event taxonomy and reporting approach across infusion reactions, treatment interruptions, escalation events, near-misses, and other clinically relevant incidents. • Own the clinical review and quality assurance process supporting accurate safety event capture from clinical documentation and operational workflows. • Produce recurring safety trend reports for clinical leadership, including root-cause themes, emerging risks, and recommendations for process improvement. • Build patient-level adherence monitoring across therapies, conditions, and populations. • Define infusion-specific adherence methodology — persistence, schedule conformance, dose fidelity, treatment completion, and tolerability — rather than retail-pharmacy measures like PDC or MPR, which weren't built for HCP-administered infusion therapy. • Build a risk-flagging process that identifies patients at elevated risk for treatment interruption or discontinuation, incorporating signals such as missed infusions, delayed authorizations, site-of-care disruptions, and medication access barriers. • Partner with care teams to operationalize proactive outreach triggers for at-risk patients. • Select, adapt, and implement validated patient-reported outcome instruments appropriate for specialty infusion populations where clinically appropriate. • Partner with Engineering and Clinical Operations to implement survey delivery workflows and structured response capture. • Analyze and interpret outcomes data to generate clinically defensible evidence of program impact. • Produce outcomes reporting and evidence packages supporting employer reporting, client QBRs, payer discussions, and manufacturer partnerships.
Fairview Health Services is a healthcare nonprofit that provides various health services, including primary care, specialized medical treatment, mental health s
Role Description Fairview has an exciting opportunity for a RN Clinic Specialist to join our Endoscopy Support team. This role is a Casual position on the day shift and is 100% remote, offering the flexibility to work from home while staying connected to a collaborative clinical team. This position typically works shifts starting between 7:00 a.m. and 8:00 a.m., with end times between 5:00 p.m. and 6:00 p.m. Flexibility to provide lunch-time coverage as required is expected. We’re proud to support a healthy work–life balance, with a predictable daytime schedule, reduced FTE for added flexibility, and a remote work environment designed to help you thrive both professionally and personally. This position is ideal for an experienced nurse who values meaningful work, team connection, and the ability to maintain balance outside of work. This specialized Registered Nurse performs both independent nursing and delegated medical functions: - Independent nursing includes assessment, planning, delivery, and evaluation of nursing care for assigned patient population(s) usually in specialty or acute care clinics. - Delegated medical function includes participation in and coordination of delegated patient care to other health care team members. - Responsible for performing these functions in accordance with all policy, procedure, and professional practice guidelines. - Assists provider with complex procedures and independently completes a variety of tasks including, but not limited to: - Injections - Phone triage - Preparation of education materials - Patient education - Patient vital checks - Chart documentation - Monitors standards of care - Keeps up to date on technological advances and new pharmaceutical products. Qualifications - Associates Degree in Nursing or Bachelor of Science Nursing - Specialty training or graduate classes related to clinical area of practice - 5 years of hospital or clinic experience or 2 years of specialty/critical care experience with specialty certification - Basic Life Support (American Heart Assoc or Red Cross) Benefits - Generous benefit package including but not limited to: - Medical, dental, vision plans - Life insurance - Short-term and long-term disability insurance - PTO and Sick and Safe Time - Tuition reimbursement - Retirement - Early access to earned wages - And more! Compensation Disclaimer An individual's pay rate within the posted range may be determined by various factors, including skills, knowledge, relevant education, experience, and market conditions. Additionally, our organization prioritizes pay equity and considers internal team equity when making any offer. Hiring at the maximum of the range is not typical. If your role is eligible for a sign-on bonus, the bonus program that is approved and in place at the time of offer, is what will be honored. EEO Statement EEO/Vet/Disabled: All qualified applicants will receive consideration without regard to any lawfully protected status.
Preserving, Creating & Facilitating
• Generate comprehensive first-level, second-level, and escalated appeal letters for denied claims. • Develop compelling clinical arguments using medical records, physician documentation, industry standards, and payer policies. • Create appeal packages with all required supporting documentation and submit within payer timelines. • Track appeal status, deadlines, and outcomes to ensure timely follow-up. • Review and revise appeal content to improve quality, consistency, and overturn success rates. • Review and assess denials related to: • Medical necessity • Level of care • Clinical validation • Authorization issues • Audit findings • Conduct detailed chart reviews to validate payer rationale and determine appeal viability. • Analyze denial trends and identify opportunities for overturn and prevention. • Apply CMS regulations, Medicare guidelines, LCDs, NCDs, payer policies, and industry guidance to support appeal arguments. • Maintain current knowledge of ICD-10-CM/PCS coding requirements, DRG methodologies, and reimbursement regulations. • Monitor payer updates and regulatory changes impacting denials and appeals. • Assist in developing appeal templates, reference materials, and best practices. • Provide recommendations to improve appeal effectiveness and reduce future denials. • Contribute to denial prevention initiatives through trend analysis and education. • Partner with physicians, CDI specialists, case management, utilization review, coding, and HIM teams to strengthen appeal outcomes.
• Provide case support to physicians within certain territories. • Cover procedural case coverage for peripheral and coronary interventional procedures in the pre-market and post-market phases. • Play a critical role in clinical studies including device training, case support, • Ensure timely data collection for clinical programs. • Present clinical study training materials based on investigational plans to support the safe and effective use of medical devices. • Manage key study investigators and foster relationships with medical advisors. • Partner with clinical research colleagues to meet business needs including site re-training and data collection. • Administrative activities including training to procedures, manage territory travel and budgets.
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• 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
We are a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health.
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
• Provide case support to physicians within certain territories. • Case support on peripheral and coronary interventional procedures in the pre-market and post-market phases of product development with the Shockwave Medical Intravascular Lithotripsy (IVL) technology. • Play a critical role in clinical studies including device training, case support, and ensuring timely data collection for clinical programs. • Manage key study investigators; foster and maintain strong relationships through direct interactions with medical advisors and clinical leaders. • Partner with other clinical research colleagues to meet business needs in the field including site re-training, data collection for timely database locks and resolution of critical issues. • Administrative activities including training to procedures, manage territory travel, and budgets. • Other duties as assigned.
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• 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
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• 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.
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