The role involves performing penetration testing across web, mobile, and API environments to identify and remediate security vulnerabilities. Additionally, the engineer will build automation tools and KPI dashboards to integrate security into DevSecOps workflows.
Clario
37 Remote Job Openings at Clario
Design, develop, and maintain scalable automated test frameworks across UI, API, and database layers. Integrate these tests into CI/CD pipelines and collaborate with cross-functional teams to ensure software quality and release readiness.
Design and develop AI-powered applications focusing on Agentic AI, LLM workflows, and scalable production services. You will be responsible for the full software development lifecycle, including model training, fine-tuning, and deployment in cloud environments.
Drive robust software deployments, infrastructure automation, and DevOps best practices to support scalable and secure clinical research platforms. Partner with engineering and IT teams to implement CI/CD pipelines and provide Tier III support for application functionality.
Acts as the primary liaison between sponsors and technical teams to gather requirements and develop specifications for data management solutions. Responsible for overseeing data integration, designing custom reports, and ensuring high-quality, compliant data delivery for clinical trials.
Lead the planning, execution, and delivery of clinical projects while ensuring compliance with regulatory and quality standards. Manage project timelines, budgets, and cross-functional teams to deliver high-quality outcomes for sponsors.
The Project Coordinator supports the delivery of clinical trials by coordinating eCOA study activities and managing digital data collection solutions. Key duties include maintaining study documentation, tracking devices, and collaborating with cross-functional teams to ensure efficient study execution.
The role involves collaborating with cross-functional teams to develop pricing estimates, budgets, and proposal documentation for clinical trial projects. Additionally, the specialist will manage change orders, maintain internal budget systems, and mentor junior team members.
Support the execution of eCOA projects by coordinating timelines, tracking deliverables, and facilitating communication across teams. Assist with study management phases including database setup, documentation development, and issue tracking.
Design and execute manual and automated testing activities for enterprise software applications to ensure quality and reliability. Collaborate with cross-functional teams to define test coverage, investigate defects, and support Agile development ceremonies.
Design, develop, and maintain high-quality mobile applications for clinical research using C# and .NET MAUI/Xamarin. You will lead architectural decisions, implement MVVM patterns, and collaborate with cross-functional teams to ensure data integrity and system scalability.
Lead the delivery of client projects by managing staff, ensuring high-quality outcomes, and maintaining budget and timeline compliance. Oversee the full project lifecycle from planning to closeout while fostering team development and customer satisfaction.
The Clinical Project Manager defines and executes project plans to ensure the unbiased evaluation of clinical trial events. This includes managing cross-functional teams, overseeing financial aspects like billing and forecasting, and ensuring adherence to SOPs and regulatory guidelines.
The role involves designing, developing, and maintaining complex SQL queries, stored procedures, and ETL processes to ensure data integrity. The developer will also optimize database performance and collaborate with cross-functional teams to support reporting and analytics needs.
Define and execute product strategies and roadmaps for patient-centric software and data platforms in the healthcare sector. Collaborate with cross-functional teams to translate complex clinical workflows into intuitive digital solutions and measurable outcomes.
The role involves designing, developing, and executing automated test scripts for web and mobile applications within an Agile environment. It also requires ensuring compliance with FDA and GxP regulations while collaborating with cross-functional teams to deliver high-quality software.
The Clinical Project Manager will lead and deliver clinical projects from start-up to close-out, ensuring high-quality execution and collaboration. Responsibilities include managing timelines, resources, financial aspects, and compliance with regulatory guidelines.
Lead the planning and delivery of strategic AI initiatives while guiding a team of AI and software engineers. Partner with cross-functional stakeholders to translate business priorities into technical roadmaps and high-quality AI solutions.
Drive new business growth for eCOA Neuroscience solutions by developing sales strategies and managing the full sales cycle from lead generation to contracting. Partner with field teams and internal stakeholders to align business development commitments with operational execution.
The Medical Writer is responsible for developing high-quality clinical documentation, including site manuals and charters, while ensuring compliance with regulatory standards. They will review study protocols, eCRFs, and SOPs to maintain accuracy and consistency across clinical studies.
Support Data Managers in day-to-day clinical data activities, including data processing, cleaning, and quality checking of study output files. Maintain study documentation and act as the primary contact for client reconciliation feedback to ensure timely resolution of data issues.
The Clinical Scientist serves as the primary scientific point of contact for international clinical trials, ensuring scientific integrity and quality delivery of services. They co-lead projects with Project Management, managing study metrics, rater training, and communication with sponsors and internal stakeholders.
Collaborate with multidisciplinary teams to support PET and SPECT imaging deployment and data analysis for neuroscience clinical trials. Lead the execution of image processing workflows and contribute to scientific publications and innovation initiatives.
Collaborate with multidisciplinary teams to deploy and analyze PET and SPECT imaging for neuroscience clinical trials. Lead the execution of image processing workflows and contribute to scientific publications and innovation initiatives.
Responsible for creating pricing estimates and change order documentation for clinical trial projects. Collaborates with Sales and Project Management teams to develop budgets and proposals based on client RFPs.
The role involves reviewing and evaluating clinical data from imaging components to ensure accuracy and consistency across multiple therapeutic areas. Responsibilities include defining data management workflows, executing edit checks, and collaborating with cross-functional teams to resolve data discrepancies.
Design, develop, and maintain scalable software applications and backend database logic across the full software development lifecycle. Collaborate with cross-functional teams in an Agile environment to troubleshoot production issues and implement product enhancements.
The Medical Oncologist provides expert medical review, data interpretation, and quality oversight for oncology-focused clinical trials. This includes interpreting clinical data according to GCP guidelines and collaborating with sponsors and regulatory stakeholders to ensure compliant deliverables.
Provide scientific and medical leadership in cardiac safety and efficacy solutions for pharmaceutical sponsors and regulatory bodies. Act as a subject-matter expert in cardiology and digital physiology to support clinical research and internal innovation.
Lead a senior engineering team in developing reusable libraries and platform capabilities to enable scalable software delivery. Drive the adoption of modern engineering practices, secure SDLC, and provide Level 4 escalation support for complex production issues.
Coordinate site and operational activities for global clinical trials from start-up to close. Perform Imaging Quality Control (IQC) activities and maintain study databases to ensure data accuracy and compliance.
Design and maintain scalable data architectures and pipelines to support clinical trial operations and business intelligence. Collaborate with cross-functional teams to integrate LLM-powered solutions and ensure data quality and governance.
Lead an engineering team in developing and maintaining shared services and high-volume APIs for clinical trial technologies. Act as a player-coach who contributes directly to the codebase while driving architectural standards and the adoption of AI-augmented workflows.
The AI Engineering Team Lead will oversee the delivery of strategic AI initiatives and manage cross-functional project teams. They are responsible for translating business priorities into technical roadmaps while mentoring engineers and ensuring high-quality, scalable AI solutions.
The Category Manager will develop and execute strategic sourcing strategies for professional services categories including HR, Legal, and Finance. They will lead procurement initiatives, negotiate contracts, and manage supplier relationships to ensure operational efficiency and cost savings.
This role coordinates and manages assigned Quality Management regulatory inspection and audit activities, supporting management and evaluation of potential regulatory concerns to ensure compliance with regulatory authorities. The analyst will support inspection execution across all regions, manage issues for continuous improvement, and assist with hosting regulatory inspections for clients.
The role involves architecting, owning, and evolving the end-to-end automated testing strategy across UI, API, integration, performance, and security testing, while designing and implementing AI-assisted test creation using LLMs. This person will also establish and promote BDD and TDD practices and mentor other engineers on quality engineering best practices.
