July 10, 2026
Business Development Representative - EdTech
Junior • Remote
60,000 - 90,000 USD/yr
Albuquerque, NM
Securly is the market leader in AI-powered student safety and wellness solutions, trusted by more than 20 million students across 20,000+ schools worldwide. Its platform combines AI and human insight to help schools proactively identify and respond to risks such as bullying, self-harm, and violence.
Securly is recognized as an EdTech Top 40 "Most Used Product" and a GSV 150 honoree.
Overview of the Role
As a Business Development Representative (BDR/SDR) at Securly, you will identify, qualify, and engage prospective school districts through cold calling and outbound strategies. The role focuses on driving pipeline growth, building relationships, and supporting long-term partnerships with school leaders nationwide.
Reports to: Director of Business Development
Core Hours: 8 - 5 pm Mountain Time Zone
Performance Objectives (First 12 Months)
- Ramp on Securly's product suite, ICPs, messaging, and internal tools
- Begin daily outreach (50–100 calls, 50–200 emails)
- Enter 10–30 new prospects into Salesforce daily
- Drive 10–25 meaningful conversations per week with K–12 contacts
- Schedule 5–15 qualified meetings weekly
- Create 8–15 new sales opportunities monthly
- Achieve a 20–30% lead-to-opportunity conversion rate
- Execute and optimize outbound prospecting across phone, email, and LinkedIn
- Leverage coaching, peer feedback, and metrics to improve performance
- Meet or exceed quota consistently
- Contribute to team best practices and support onboarding of new BDRs
Core Responsibilities
- Drive high-volume, multi-touch outreach via phone, email, and LinkedIn to engage K–12 decision-makers
- Qualify inbound and outbound leads based on interest, urgency, and fit
- Deliver compelling product messaging using testimonials, outcomes, and market data
- Handle objections and tailor conversations to prospect priorities
- Maintain clean and accurate records in Salesforce and Outreach.io
- Partner with Sales, Marketing, and RevOps to ensure seamless handoff of qualified leads
- Continuously improve through coaching, data insights, and collaboration with peers
Qualifications
- Experience in high-activity outbound sales roles
- Experience with SaaS or EdTech preferred
- Strong communication and active listening skills
- Experience using Salesforce and Outreach.io
- Ability to research prospects and personalize outreach
- Experience maintaining organized CRM records and pipeline management
- Ability to collaborate with Sales and Marketing teams
- Understanding of K–12 structures and stakeholder roles
Tools & Technology You'll Use
- Salesforce
- Outreach.io
- GovSpend
- AI Gems
Compensation & Benefits
- Total Compensation: $60,000 base + $30,000 variable = $90,000 OTE
- Medical, dental, and vision coverage
- 401(k) with company match
- Unlimited PTO
- 12 weeks paid parental leave
- Year-end paid shutdown
- 24/7 confidential mental health counseling and wellness tools
- $1,000 annual learning stipend
- Structured onboarding and coaching
Securly is an Equal Opportunity Employer committed to building a diverse, inclusive workplace.
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Focus on user and business outcomes, not output. Core requirements 1+ year of software development experience building something real (product, system, tool, startup, side project, meaningful feature, or student project) You value autonomy over stability and process You enjoy working across layers instead of staying in one box You think in problems and outcomes, not tickets You are comfortable with ambiguity You can learn new technologies quickly You are curious about AI and excited to work with agents Tools You Will Use Backend: Go, MySQL, Kafka, Docker, Kubernetes, AWS, Redis Frontend: Next.js, React.js , TypeScript, GraphQL, Tailwind CSS, Cloudflare Workers IOS: SwiftUI, Xcode, Combine, SPM, MVVM Architecture Android: Kotlin, Android Studio, Hilt, Coroutines, Jetpack Compose, MVVM Architecture Infra: Linux, Docker, GitLab, ArgoCD, AWS, Terraform, Helm, OpenSearch, Prometheus, Python / Golang AI tools: Claude Code, OpenAI Codex, OpenCode, Cursor with Composer Salary Range Gross salary: 18,100 — 24,400 PLN / month What We Offer Innovate with industry leaders Work alongside global experts to build world-leading cybersecurity tools, impacting millions of users around the world. Learn & grow Boost your skills via our extensive training programs (online and offline) & other resources. Benefit from mentorship and career-switch opportunities to grow within the company. Hybrid work Enjoy the flexibility with 3 office days and working from home for the remaining 2. Work from anywhere Recharge with a change of scenery – choose work from any location when you feel a need to power your creativity and drive. Physical well-being Fuel your active lifestyle with online workouts led by our Physical Well-Being experts. Unlock a variety of sports and wellness facilities, like gyms, swimming pools, and fitness classes, with the Multisport card. Mental & emotional health Nurture your mind with free psychologist consultations, dedicated mental health events, and premium access to top-rated wellness apps like Calm, Headspace, and Mindletic. Premium healthcare Receive private health insurance giving you peace of mind for your health needs. Joyful moments – special treats Celebrate life’s big moments with special gifts from us on your birthday, anniversary, and other major events, such as weddings or the arrival of a new family member. Company events & team-building Experience iconic Nord Security celebrations, team-buildings, and knowledge-sharing events, nurturing bonds that fuel our success. Workation Embark on a legendary company getaway abroad, filled with exciting activities, live concerts, engaging workshops, and epic time together.
Technology

Cleerly
Senior Software V&V Engineer, Imaging Systems
Senior
Remote
Denver, CO
176,004 - 206,004 USD/yr
🏢 Summary: Software Verification and Validation Engineer role focused on ensuring quality, safety, and regulatory compliance of AI-driven medical imaging software products. The position involves leading V&V planning, developing test strategies and protocols, supporting software development cycles, and collaborating with cross-functional teams in a regulated medical device environment. 🗂️ Requirements: 5+ years of experience in the medical imaging industry, Bachelor's or Master's degree in Computer Science, Information Technology, or related field, Experience with non-product software development, Strong Python programming skills, Experience with quality engineering regulations and standards, Experience with JIRA or similar project management tools, Understanding of SDLC and software testing lifecycle, Ability to collaborate in remote-first teams, Strong analytical and problem-solving skills 📃 Skills: Python, JIRA, AWS, SCRUM, FDA, ISO13485, ISO14971, IEC62304, MDSAP, MDR, QSR 🏢 Description: About Cleerly We're Cleerly – a healthcare company that's revolutionizing how heart disease is diagnosed, treated, and tracked. We were founded in 2017 by one of the world's leading cardiologists and are a growing team of world-class engineering, operations, medical affairs, marketing, and sales leaders. Cleerly has created a new standard of care for heart disease through value-based, AI-driven precision diagnostic solutions with the goal of helping prevent heart attacks. Our technology goes beyond traditional measures of heart disease by enabling comprehensive quantification and characterization of atherosclerosis, or plaque buildup, in each of the heart arteries. At Cleerly, we collaborate digitally and use a wide variety of systems. Our people use Google Workspace (GMail, Drive, Docs, Sheets, Slides), Slack, Confluence/Jira, and Zoom Video, prior experience in these areas is a plus. While we are mostly a remote company, travel is required for some team meetings and cross function projects typically once per month or once per quarter. Cleerly is committed to providing safe and effective medical software that meets customer needs and our intended use. The adherence to all applicable regulatory and statutory requirements establishes a clear framework for setting measurable quality objectives. About the Opportunity We are seeking a software verification and validation (V&V) engineer to ensure the quality of cutting-edge products to meet all defined system and subsystem level requirements and are safe, effective, and compliant for their intended clinical use. This role plays a critical part in supporting regulatory submissions and product releases by planning, executing, and documenting comprehensive V&V activities in accordance with FDA regulations, ISO 13485, IEC standards, and other applicable regulatory and quality system requirements. Key Responsibilities - Develop and lead the Design Verification and Validation (V&V) plan in compliance with regulatory and quality system requirements (21 CFR Part 820, ISO 13485, ISO 14971) - Define test strategies, protocols, and acceptance criteria for mechanical, electrical, optical, and system-level performance - Build complex data sets to be used in testing - Perform statistical analysis and exploratory data analysis including descriptive statistics, regression, and visualization - Develop test methods and verification protocols for software products - Create and maintain test master plans, schedules, and resource allocation for multiple device programs - Participate in software development sprint cycles by attending SCRUMs, design reviews, and code reviews - Collaborate with cross-functional teams to translate requirements into comprehensive test plans and protocols - Support data governance, access controls, and PHI data handling Required Qualifications & Skills - 5+ years equivalent work experience in the medical imaging industry (Product Development, Quality) - Bachelor's or Master's degree in Computer Science, Information Technology, or related field - Experience with non-product software development - Strong programming skills in Python across data science, statistical analysis, big data, and ML stack - Experience with quality engineering under quality system regulations, including 21 CFR Part 820, ISO 14971, IEC 62304, QSR, ISO 13485, MDSAP, and/or MDD/MDR - Expertise in issue tracking and project management tools like JIRA - Strong understanding of the software development life cycle and testing life cycle - Excellent problem-solving, analytical, and critical thinking skills - Ability to work collaboratively in a remote-first team environment and communicate effectively with stakeholders Preferred Qualifications - Prior experience utilizing AWS Cloud Services or equivalent enterprise cloud service providers - Experience in Class II or Class III medical devices preferred - Experience in cardiovascular imaging systems is a plus Compensation - Base Salary: $153,000 - $179,000 - Total Target Compensation (TTC): $176,000 - $206,000 - Eligible for a 15% target annual bonus - Stock options, paid benefits, and employee perks included as part of total rewards Core Values - Humility – be a servant leader - Excellence – deliver world-changing results - Accountability – do what you say; expect the same from others - Remarkable – inspire and innovate with impact - Teamwork – together we win
Technology

Cleerly
Senior Software V&V Engineer, Imaging Systems
Senior
Remote
176,004 - 206,004 USD/yr
🏢 Summary: Software Verification and Validation Engineer role focused on ensuring quality, compliance, and safety of AI-driven medical imaging products through comprehensive V&V activities. The position involves developing test plans and protocols, supporting software development cycles, performing statistical and data analysis, and ensuring compliance with FDA and ISO standards. Candidates should have strong Python, quality engineering, and medical device software validation experience. 🗂️ Requirements: 5+ years experience in medical imaging industry product development or quality, Bachelor's or Master's degree in Computer Science, Information Technology, or related field, Experience with non-product software development, Strong Python programming skills, Experience with statistical analysis and exploratory data analysis, Experience with software verification and validation test methods and protocols, Knowledge of 21 CFR Part 820, ISO 14971, IEC 62304, QSR, ISO 13485, MDSAP, MDD/MDR, Experience with JIRA or similar project management tools, Understanding of software development lifecycle and testing lifecycle, Ability to collaborate in remote-first cross-functional teams 📃 Skills: Python, JIRA, AWS, SCRUM, ISO13485, ISO14971, IEC62304, QSR, MDSAP, MDR, FDA, Statistics, ML, Testing, Validation, Verification 🏢 Description: About the Opportunity We are seeking a software verification and validation (V&V) engineer to ensure the quality of cutting-edge products to meet all defined system and subsystem level requirements and are safe, effective, and compliant for their intended clinical use. This role plays a critical part in supporting regulatory submissions and product releases by planning, executing, and documenting comprehensive V&V activities in accordance with FDA regulations, ISO 13485, IEC standards, and other applicable regulatory and quality system requirements. Key Responsibilities - Develop and lead the Design Verification and Validation (V&V) plan in compliance with regulatory and quality system requirements (21 CFR Part 820, ISO 13485, ISO 14971). - Define test strategies, protocols, and acceptance criteria for mechanical, electrical, optical, and system-level performance. - Build complex data sets to be used in test. - Perform statistical analysis and exploratory data analysis, including descriptive statistics, regression, and visualization. - Develop test methods and verification protocols for software products. - Create and maintain test master plans, schedules, and resource allocation for multiple device programs. - Participate in software development sprint cycles by supporting the software development team through SCRUMs, design reviews, code reviews, and feedback on software verification and validation deliverables. - Collaborate with cross-functional teams to understand requirements and translate them into comprehensive test plans and protocols. - Support data governance, access controls, and PHI data handling. Required Qualifications & Skills - 5+ years equivalent work experience in medical imaging industry (Product Development, Quality). - Bachelor's or Master's degree in Computer Science, Information Technology, or related field. - Experience with non-product software development. - Strong programming skills in Python across data science, statistical analysis, big data, and ML stack. - Experience with quality engineering under quality system regulations, including but not limited to 21 CFR Part 820, ISO 14971, IEC 62304, QSR, ISO 13485, MDSAP, and/or MDD/MDR. - Expertise in issue tracking and project management tools like JIRA. - Strong understanding of the software development life cycle and testing life cycle. - Excellent problem-solving, analytical, and critical thinking skills. - Ability to work collaboratively in a remote-first team environment and communicate effectively with Product Managers, Engineers, and stakeholders. Preferred Qualifications - Prior experience utilizing AWS Cloud Services or equivalent enterprise cloud service provider. - Experience in Class II or Class III medical devices preferred. - Experience in cardiovascular imaging systems is a major plus. Compensation and Benefits - Base Salary: $153,000 - $179,000. - Total Target Compensation: $176,000 - $206,000. - Eligible for 15% target annual bonus. - Stock options, paid benefits, and employee perks included as part of total rewards. - Remote-first work environment with occasional travel for meetings and projects. Additional Information - Job duties, activities, and responsibilities are subject to change. - Equal opportunity employer.
Healthcare

Cleerly
Senior Software V&V Engineer, Imaging Systems
Senior
Remote
Denver, CO
176,004 - 206,004 USD/yr
🏢 Summary: Software Verification & Validation (V&V) Engineer responsible for ensuring medical software products meet system requirements and regulatory standards for safe clinical use. The role involves planning and executing verification strategies, developing test protocols, performing statistical analysis, and supporting regulatory submissions in compliance with FDA and ISO standards. You will collaborate with cross-functional teams within an agile environment to deliver high-quality, compliant medical imaging software. 🗂️ Requirements: 5+ years experience in medical imaging product development or quality, Bachelor’s or Master’s degree in Computer Science, Information Technology, or related field, Experience with non-product software development, Strong Python programming for data science, statistical analysis, big data and ML, Experience working under 21 CFR Part 820, ISO 13485, ISO 14971, IEC 62304, QSR or related regulations, Experience with JIRA for issue tracking and project management, Strong understanding of SDLC and software testing lifecycle, Experience developing verification protocols and test methods for software products 📃 Skills: Python, AWS, JIRA, ISO13485, ISO14971, IEC62304, QSR, MDSAP, MDR, FDA, SDLC, SCRUM, Statistics, EDA, MachineLearning, DataAnalysis 🏢 Description: About Cleerly We're Cleerly – a healthcare company that's revolutionizing how heart disease is diagnosed, treated, and tracked. We were founded in 2017 by one of the world's leading cardiologists and are a growing team of world-class engineering, operations, medical affairs, marketing, and sales leaders. We raised $223M in Series C funding in 2022 which has enabled rapid growth and continued support of our mission. In December 2024 we received an additional $106M in a Series C extension funding. Most of our teams work remotely and have access to our offices in Denver, Colorado, New, York, New York, Dallas, Texas, and Lisbon, Portugal with some roles requiring you to be on-site in a location. Cleerly has created a new standard of care for heart disease through value-based, AI-driven precision diagnostic solutions with the goal of helping prevent heart attacks. Our technology goes beyond traditional measures of heart disease by enabling comprehensive quantification and characterization of atherosclerosis, or plaque buildup, in each of the heart arteries. Cleerly's solutions are supported by more than a decade of performing some of the world's largest clinical trials to identify important findings beyond symptoms that increase a person's risk of heart attacks. At Cleerly, we collaborate digitally and use a wide variety of systems. Our people use Google Workspace (GMail, Drive, Docs, Sheets, Slides), Slack, Confluence/Jira, and Zoom Video, prior experience in these areas is a plus. Role or department specific technology needs may vary and will be listed as requirements in the job description. While we are mostly a remote company, travel is required for some team meetings and cross function projects typically once per month or once per quarter, for some roles like sales or external facing roles travel could be up to 90% of the time. Cleerly is committed to providing safe and effective medical software that meets customer needs and our intended use. The adherence to all applicable regulatory and statutory requirements establishes a clear framework for setting measurable quality objectives. Our commitment to continually improving our products and processes proactively manages risks, ensuring ongoing compliance throughout the entire software lifecycle. Understanding this role's relevance and importance is critical to achieving Cleerly's quality objectives. About the Opportunity We are seeking a software verification and validation (V&V) engineer to ensure the quality of cutting-edge products to meet all defined system and subsystem level requirements and are safe, effective, and compliant for their intended clinical use. This role plays a critical part in supporting regulatory submissions and product releases by planning, executing, and documenting comprehensive V&V activities in accordance with FDA regulations, ISO 13485, IEC standards, and other applicable regulatory and quality system requirements. Key Responsibilities Develop and lead the Design Verification and Validation (V&V) plan in compliance with regulatory and quality system requirements (21 CFR Part 820, ISO 13485, ISO 14971). Define test strategies, protocols, and acceptance criteria for mechanical, electrical, optical, and system-level performance. Build complex data sets to be used in test Statistical Analysis and Exploratory Data Analysis (e.g., descriptive statistics, regression, visualization) Developed test methods and verification protocols for software product Create and maintain test master plans, schedules, and resource allocation for multiple device programs. Participate in software development sprint cycles by supporting the software development team through attending SCRUMs, design reviews, code reviews and providing feedback on software verification and validation deliverables. Collaborate with cross-functional teams to understand requirements and translate them into comprehensive test plans and protocols Data Governance, Access Controls, and PHI Data Handling Responsibilities Required Qualifications & Skills 5+ years equivalent work experience in medical imaging industry(Product Development, Quality) Bachelor's or Master's degree in Computer Science, Information Technology, or related field. Experience with non-product software development Strong programming skills in Python across data science, statistical analysis, big data and ML stack Experience with quality engineering under quality system regulations, including but not limited to 21 CFR Part 820, ISO 14971, IEC 62304, QSR, ISO 13485, MDSAP and/or MDD/MDR Expertise in issue tracking and project management tools like JIRA Strong understanding of the software development life cycle and testing life cycle. Excellent problem-solving, analytical, and critical thinking skills Ability to work collaboratively in a remote-first team environment and to communicate effectively with Product Managers, Engineers, and other stakeholders Impress us more Prior experience in utilizing AWS Cloud Services or an equivalent enterprise cloud service provider Experience in Class II or Class III medical devices is preferred Experience in Cardiovascular imaging system is a major plus OUR COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER. We do not discriminate on the basis of race, color, national origin, ancestry, citizenship status, protected veteran status, religion, physical or mental disability, marital status, sex, sexual orientation, gender identity or expression, age, or any other basis protected by law, ordinance, or regulation. Job duties, activities, and responsibilities are subject to change by our company. The base salary range for this role varies by location and is aligned to market benchmarks. Candidates located in higher-cost labor markets, including California, Washington, New York, New Jersey, Connecticut, Massachusetts, and Washington, DC represent the middle to high end of the range, while candidates located in all other U.S. locations represent the low to middle end of the range. Final compensation is determined based on location, experience, skills, and internal equity. This role is eligible for a 15% target annual bonus, resulting in the following base salary and Total Target Compensation (TTC) ranges: Base Salary: $153,000 - $179000 TTC: $176,000 - $206,000 *Total Target Compensation (TTC): Total Cash Compensation (including base pay, variable pay, commission, bonuses, etc.) Additionally, stock options, paid benefits, and employee perks are part of your total rewards.Working at Cleerly takes HEART. Discover our Core Values: H: Humility- be a servant leader E: Excellence- deliver world-changing results A: Accountability- do what you say; expect the same from others R: Remarkable- inspire & innovate with impact T: Teamwork- together we win Don't meet 100 percent of the qualifications? Apply anyway and help us diversify our candidate pool and workforce. We value experience, whether gained formally or informally on the job or through other experiences. Job duties, activities and responsibilities are subject to change by our company. OUR COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER. We do not discriminate on the basis of race, color, national origin, ancestry, citizenship status, protected veteran status, religion, physical or mental disability, marital status, sex, sexual orientation, gender identity or expression, age, or any other basis protected by law, ordinance, or regulation. For more information see our Privacy Policy (https://cleerlyhealth.com/privacy-policy). All official emails will come from @cleerlyhealth.com email accounts. #Cleerly
Healthcare

Cleerly
Senior Software V&V Engineer, Imaging Systems
Senior
Remote
176,004 - 206,004 USD/yr
🏢 Summary: Software Verification & Validation (V&V) Engineer responsible for ensuring medical software products meet system requirements and regulatory standards for safe clinical use. The role involves planning and executing comprehensive V&V activities, supporting FDA submissions, and collaborating with cross-functional teams within an AI-driven medical imaging environment. Strong focus on regulatory compliance, software testing, and data-driven validation. 🗂️ Requirements: 5+ years experience in medical imaging industry (Product Development or Quality), Bachelor’s or Master’s degree in Computer Science, Information Technology, or related field, Experience with non-product software development, Strong Python programming skills for data science and statistical analysis, Experience working under 21 CFR Part 820, ISO 13485, ISO 14971, IEC 62304 or similar regulations, Experience with JIRA or similar issue tracking tools, Strong understanding of SDLC and STLC, Experience in software verification and validation processes 📃 Skills: Python, FDA, ISO13485, ISO14971, IEC62304, QSR, MDSAP, MDR, JIRA, AWS, SDLC, STLC, SCRUM, Statistics, ML, DataAnalysis 🏢 Description: About Cleerly We're Cleerly – a healthcare company that's revolutionizing how heart disease is diagnosed, treated, and tracked. We were founded in 2017 by one of the world's leading cardiologists and are a growing team of world-class engineering, operations, medical affairs, marketing, and sales leaders. We raised $223M in Series C funding in 2022 which has enabled rapid growth and continued support of our mission. In December 2024 we received an additional $106M in a Series C extension funding. Most of our teams work remotely and have access to our offices in Denver, Colorado, New, York, New York, Dallas, Texas, and Lisbon, Portugal with some roles requiring you to be on-site in a location. Cleerly has created a new standard of care for heart disease through value-based, AI-driven precision diagnostic solutions with the goal of helping prevent heart attacks. Our technology goes beyond traditional measures of heart disease by enabling comprehensive quantification and characterization of atherosclerosis, or plaque buildup, in each of the heart arteries. Cleerly's solutions are supported by more than a decade of performing some of the world's largest clinical trials to identify important findings beyond symptoms that increase a person's risk of heart attacks. At Cleerly, we collaborate digitally and use a wide variety of systems. Our people use Google Workspace (GMail, Drive, Docs, Sheets, Slides), Slack, Confluence/Jira, and Zoom Video, prior experience in these areas is a plus. Role or department specific technology needs may vary and will be listed as requirements in the job description. While we are mostly a remote company, travel is required for some team meetings and cross function projects typically once per month or once per quarter, for some roles like sales or external facing roles travel could be up to 90% of the time. Cleerly is committed to providing safe and effective medical software that meets customer needs and our intended use. The adherence to all applicable regulatory and statutory requirements establishes a clear framework for setting measurable quality objectives. Our commitment to continually improving our products and processes proactively manages risks, ensuring ongoing compliance throughout the entire software lifecycle. Understanding this role's relevance and importance is critical to achieving Cleerly's quality objectives. About the Opportunity We are seeking a software verification and validation (V&V) engineer to ensure the quality of cutting-edge products to meet all defined system and subsystem level requirements and are safe, effective, and compliant for their intended clinical use. This role plays a critical part in supporting regulatory submissions and product releases by planning, executing, and documenting comprehensive V&V activities in accordance with FDA regulations, ISO 13485, IEC standards, and other applicable regulatory and quality system requirements. Key Responsibilities Develop and lead the Design Verification and Validation (V&V) plan in compliance with regulatory and quality system requirements (21 CFR Part 820, ISO 13485, ISO 14971). Define test strategies, protocols, and acceptance criteria for mechanical, electrical, optical, and system-level performance. Build complex data sets to be used in test Statistical Analysis and Exploratory Data Analysis (e.g., descriptive statistics, regression, visualization) Developed test methods and verification protocols for software product Create and maintain test master plans, schedules, and resource allocation for multiple device programs. Participate in software development sprint cycles by supporting the software development team through attending SCRUMs, design reviews, code reviews and providing feedback on software verification and validation deliverables. Collaborate with cross-functional teams to understand requirements and translate them into comprehensive test plans and protocols Data Governance, Access Controls, and PHI Data Handling Responsibilities Required Qualifications & Skills 5+ years equivalent work experience in medical imaging industry(Product Development, Quality) Bachelor's or Master's degree in Computer Science, Information Technology, or related field. Experience with non-product software development Strong programming skills in Python across data science, statistical analysis, big data and ML stack Experience with quality engineering under quality system regulations, including but not limited to 21 CFR Part 820, ISO 14971, IEC 62304, QSR, ISO 13485, MDSAP and/or MDD/MDR Expertise in issue tracking and project management tools like JIRA Strong understanding of the software development life cycle and testing life cycle. Excellent problem-solving, analytical, and critical thinking skills Ability to work collaboratively in a remote-first team environment and to communicate effectively with Product Managers, Engineers, and other stakeholders Impress us more Prior experience in utilizing AWS Cloud Services or an equivalent enterprise cloud service provider Experience in Class II or Class III medical devices is preferred Experience in Cardiovascular imaging system is a major plus OUR COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER. We do not discriminate on the basis of race, color, national origin, ancestry, citizenship status, protected veteran status, religion, physical or mental disability, marital status, sex, sexual orientation, gender identity or expression, age, or any other basis protected by law, ordinance, or regulation. Job duties, activities, and responsibilities are subject to change by our company. The base salary range for this role varies by location and is aligned to market benchmarks. Candidates located in higher-cost labor markets, including California, Washington, New York, New Jersey, Connecticut, Massachusetts, and Washington, DC represent the middle to high end of the range, while candidates located in all other U.S. locations represent the low to middle end of the range. Final compensation is determined based on location, experience, skills, and internal equity. This role is eligible for a 15% target annual bonus, resulting in the following base salary and Total Target Compensation (TTC) ranges: Base Salary: $153,000 - $179000 TTC: $176,000 - $206,000 *Total Target Compensation (TTC): Total Cash Compensation (including base pay, variable pay, commission, bonuses, etc.) Additionally, stock options, paid benefits, and employee perks are part of your total rewards.Working at Cleerly takes HEART. Discover our Core Values: H: Humility- be a servant leader E: Excellence- deliver world-changing results A: Accountability- do what you say; expect the same from others R: Remarkable- inspire & innovate with impact T: Teamwork- together we win Don't meet 100 percent of the qualifications? Apply anyway and help us diversify our candidate pool and workforce. We value experience, whether gained formally or informally on the job or through other experiences. Job duties, activities and responsibilities are subject to change by our company. OUR COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER. We do not discriminate on the basis of race, color, national origin, ancestry, citizenship status, protected veteran status, religion, physical or mental disability, marital status, sex, sexual orientation, gender identity or expression, age, or any other basis protected by law, ordinance, or regulation. For more information see our Privacy Policy (https://cleerlyhealth.com/privacy-policy). All official emails will come from @cleerlyhealth.com email accounts. #Cleerly
Technology

Cleerly
Software Engineer III
Senior
Remote
Denver, CO
141,900 - 165,204 USD/yr
🏢 Summary: Software Engineer III role focused on building and scaling enterprise-grade healthcare platforms for quantitative computer-aided diagnosis. The position involves fullstack development of secure, reliable systems using modern web technologies, backend services, and cloud infrastructure in a distributed agile environment. 🗂️ Requirements: Bachelor's or Master's degree in Computer Science, Software Engineering, or related field, 5–8 years of professional software engineering experience, Fullstack development experience, Proficiency in React, Proficiency in CSS, Proficiency in Node.js, Proficiency in TypeScript, Experience with RESTful APIs, Experience with PostgreSQL or relational databases, Understanding of software engineering practices and system design, Ability to own medium-to-large features from development to production, Strong communication and collaboration skills 📃 Skills: React, CSS, Node.js, TypeScript, REST, PostgreSQL, Next.js, Ant, Docker, AWS, EKS, CI/CD, Python, Microservices 🏢 Description: About the Opportunity We're seeking a Software Engineer III with strong fullstack skills to help scale and evolve our enterprise-grade platform for quantitative computer-aided diagnosis. In this role, you'll be a key contributor to the development of secure, reliable, and maintainable systems, delivering high-impact features and improving the foundation that powers healthcare solutions. The Operational System team owns the Core Lab Case Management platform, which is the central nervous system of laboratory operations. The team builds workflows that orchestrate the lifecycle of each case, ensuring that complex case data moves seamlessly through the lab and is categorized and prioritized correctly. By optimizing how cases are processed, operations remain scalable and COGS grows efficiently alongside the business. Requirements Qualifications - Bachelor's or Master's degree in Computer Science, Software Engineering, or related field (or equivalent experience) - 5–8 years of professional experience as a software engineer, including fullstack development - Proficiency in React, CSS, Node.js, and TypeScript - Experience designing and consuming RESTful APIs - Familiarity with relational databases like PostgreSQL - Strong understanding of modern software engineering practices, system design, and debugging - Ability to take ownership of medium-to-large features and follow through from idea to production - Effective communication and collaboration skills, especially in distributed environments Preferred - Familiarity with regulated domains such as healthcare or fintech and high-availability infrastructure - Experience with containerized cloud environments (Docker, AWS EKS), CI/CD automation, and infrastructure as code - Exposure to event-driven architecture or microservices with asynchronous workflows - Familiarity with Python is a plus Responsibilities - Develop scalable backend services using Node.js and TypeScript and performant user-facing applications using React and Next.js - Build performant, accessible, and user-friendly interfaces with modern UI frameworks such as Ant - Write testable, observable, and maintainable code that meets performance and quality standards - Participate in system design reviews and propose scalable improvements - Collaborate with product, design, and engineering teammates in an agile team environment - Contribute to documentation, code reviews, and shared engineering standards - Participate in on-call rotations and assist with triaging production issues Compensation and Benefits - Base Salary: $129,000 - $152,000 - Total Target Compensation: $141,900 - $165,200 - Eligible for a 15% target annual bonus - Stock options, paid benefits, and employee perks included as part of total rewards Additional Information - Travel may be required for team meetings and cross-functional projects, typically once per month or once per quarter - Job duties, activities, and responsibilities are subject to change