Senior SDET - Device Integrations - Full-time

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**Senior SDET – Device Integrations** **About Us** We are the creators of ClinSpark—the world’s first CDISC ODM certified Phase I eSource and clinical trial automation system. ClinSpark (also known as the 'IQVIA Clinical eSource Platform') improves the speed, quality, and transparency of clinical research. Our platform supports a large and growing set of device integrations, enabling data collected from trial subjects both onsite and remote to be immediately available for review by study teams and sponsors. As part of the Connected Devices group within IQVIA, we leverage data, technology, advanced analytics, and expertise to help customers drive healthcare—and human health—forward. Our globally distributed team works remotely, offering freedom, flexibility, and a healthy work-life balance. Family matters to us. Working here is challenging, never boring, and incredibly rewarding. Learn more about our product: https://www.iqvia.com/solutions/technologies/orchestrated-clinical-trials/patient-engagement-suite/clinical-trial-services-connected-devices **About You** You are a creative thinker who strives to find efficiencies and solve problems. You are hungry to learn, self-motivated, persistent, and detail-oriented. You have a strong technical aptitude and an innovative approach to software development and testing. You enjoy being part of cross-functional teams that build and deliver solutions. You have direct experience or a desire to work with medical devices and enable electronic data capture systems. You are passionate about contributing to projects that positively impact millions of human lives. **About the Role** You will join a globally distributed, highly professional team of domain experts, product owners, project managers, software testers, and engineers tackling all aspects of our business and operations. Your responsibilities will include: + Designing and developing software testing solutions based on business needs and requirements, primarily involving automation frameworks, scripts, and tools for testing medical device integrations (ECG, blood pressure, continuous glucose monitors, etc.). + Interfacing with a range of technologies, including USB/serial port communication, SDKs/DLLs, web-based APIs, cloud microservices, and mobile applications. + Focusing on software quality standards by performing code reviews, providing input on software features and non-functional expectations, and developing/implementing test strategies that align with user requirements and industry standards. + Ensuring efficient and effective testing processes for regression, integration, security, performance, and communicating results/metrics to stakeholders. + Evaluating new technologies and tools for potential adoption. + Analyzing and evaluating escalated issues regarding device integrations, and communicating effectively with customers. + Creating and contributing to technical documentation in support of SDLC, including software design documents, functional specifications, and change requests, as well as diagrams and visual assets to depict capabilities and workflows. + Assisting in onboarding new software engineers to the team as needed. This position is fully remote. Candidates in United States time zones will be at an advantage. **Qualifications** **Required:** + Bachelor’s Degree in Computer Science, a related field, or equivalent experience. + Minimum five (5) years of software development or software testing automation experience. + Knowledge of Software Development Life Cycle (SDLC) processes and best practices. + Demonstrated expertise in object-oriented programming (OOP), especially in Java or other similar language. + Experience developing or testing desktop, web, and/or mobile applications. + Experience in test automation tools (e.g., Playwright, Selenium, Cypress, Appium). + Experience implementing or testing system integrations via APIs, webhooks, etc. + Experience using relational database management systems, such as MySQL. + Experience using git and shell scripting. + Strong analytical and problem-solving skills. + Excellent communication and interpersonal skills. + Ability to work independently and in a remote team environment. **Nice To Have:** + Experience using Java/Groovy, JavaScript, Grails, and/or SQL. + Experience with various system communication protocols (HTTP, web sockets, SFTP, serial, Bluetooth, etc.). + Experience with various data formats (JSON, CSV, XML, HL7, etc.). + Advanced understanding of modern/scalable software architecture patterns. + Performance and security testing experience. + Experience using CI/CD pipelines and other DevOps practices. + Experience with Amazon Web Services (AWS) cloud-provider and Kubernetes infrastructure. + Knowledge of Phase I-IV clinical trial operations and workflows. + Expertise in clinical trial management software. + Knowledge of applicable clinical research, regulatory, and other requirements (e.g., Good Clinical Practice, HIPAA, GDPR, EMA, GAMP5, FDA 21 CFR Part 11). IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $91,300.00 - $228,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled
**Senior SDET – Device Integrations** **About Us** We are the creators of ClinSpark—the world’s first CDISC ODM certified Phase I eSource and clinical trial automation system. ClinSpark (also known as the 'IQVIA Clinical eSource Platform') improves the speed, quality, and transparency of clinical research. Our platform supports a large and growing set of device integrations, enabling data collected from trial subjects both onsite and remote to be immediately available for review by study teams and sponsors. As part of the Connected Devices group within IQVIA, we leverage data, technology, advanced analytics, and expertise to help customers drive healthcare—and human health—forward. Our globally distributed team works remotely, offering freedom, flexibility, and a healthy work-life balance. Family matters to us. Working here is challenging, never boring, and incredibly rewarding. Learn more about our product: https://www.iqvia.com/solutions/technologies/orchestrated-clinical-trials/patient-engagement-suite/clinical-trial-services-connected-devices **About You** You are a creative thinker who strives to find efficiencies and solve problems. You are hungry to learn, self-motivated, persistent, and detail-oriented. You have a strong technical aptitude and an innovative approach to software development and testing. You enjoy being part of cross-functional teams that build and deliver solutions. You have direct experience or a desire to work with medical devices and enable electronic data capture systems. You are passionate about contributing to projects that positively impact millions of human lives. **About the Role** You will join a globally distributed, highly professional team of domain experts, product owners, project managers, software testers, and engineers tackling all aspects of our business and operations. Your responsibilities will include: + Designing and developing software testing solutions based on business needs and requirements, primarily involving automation frameworks, scripts, and tools for testing medical device integrations (ECG, blood pressure, continuous glucose monitors, etc.). + Interfacing with a range of technologies, including USB/serial port communication, SDKs/DLLs, web-based APIs, cloud microservices, and mobile applications. + Focusing on software quality standards by performing code reviews, providing input on software features and non-functional expectations, and developing/implementing test strategies that align with user requirements and industry standards. + Ensuring efficient and effective testing processes for regression, integration, security, performance, and communicating results/metrics to stakeholders. + Evaluating new technologies and tools for potential adoption. + Analyzing and evaluating escalated issues regarding device integrations, and communicating effectively with customers. + Creating and contributing to technical documentation in support of SDLC, including software design documents, functional specifications, and change requests, as well as diagrams and visual assets to depict capabilities and workflows. + Assisting in onboarding new software engineers to the team as needed. This position is fully remote. Candidates in United States time zones will be at an advantage. **Qualifications** **Required:** + Bachelor’s Degree in Computer Science, a related field, or equivalent experience. + Minimum five (5) years of software development or software testing automation experience. + Knowledge of Software Development Life Cycle (SDLC) processes and best practices. + Demonstrated expertise in object-oriented programming (OOP), especially in Java or other similar language. + Experience developing or testing desktop, web, and/or mobile applications. + Experience in test automation tools (e.g., Playwright, Selenium, Cypress, Appium). + Experience implementing or testing system integrations via APIs, webhooks, etc. + Experience using relational database management systems, such as MySQL. + Experience using git and shell scripting. + Strong analytical and problem-solving skills. + Excellent communication and interpersonal skills. + Ability to work independently and in a remote team environment. **Nice To Have:** + Experience using Java/Groovy, JavaScript, Grails, and/or SQL. + Experience with various system communication protocols (HTTP, web sockets, SFTP, serial, Bluetooth, etc.). + Experience with various data formats (JSON, CSV, XML, HL7, etc.). + Advanced understanding of modern/scalable software architecture patterns. + Performance and security testing experience. + Experience using CI/CD pipelines and other DevOps practices. + Experience with Amazon Web Services (AWS) cloud-provider and Kubernetes infrastructure. + Knowledge of Phase I-IV clinical trial operations and workflows. + Expertise in clinical trial management software. + Knowledge of applicable clinical research, regulatory, and other requirements (e.g., Good Clinical Practice, HIPAA, GDPR, EMA, GAMP5, FDA 21 CFR Part 11). IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $91,300.00 - $228,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled
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