Jobs at Clario

Leads Clario’s global Pricing & Proposals team for its Digital Physiology business, overseeing pricing documents, proposals, Statements of Service, and change orders. Drives process optimization, system and technology adoption, KPI reporting, compliance, stakeholder relationships, and strategic initiatives. Manages team performance, career development, training, and professional growth while ensuring high-quality deliverables meet client deadlines and service-level requirements.

Manages clinical trial data throughout the study lifecycle, including data collection, cleaning, reconciliation, transfers, database lock, edit checks, and quality review. Partners with Sponsors, CROs, programming teams, and internal stakeholders to maintain Data Management Plans, specifications, documentation, timelines, and regulatory compliance. Leads study meetings, resolves data queries and corrections, supports study setup and reporting, manages escalations, and contributes to process improvement and operational excellence.

Lead the mobile delivery roadmap, mentor engineers, and establish technical direction. Design and improve CI/CD pipelines for Android and iOS applications, automate build, testing, signing, versioning, secrets, and app-store releases, and troubleshoot complex delivery issues. Partner with mobile engineering, QA, security, and product teams to improve reliability, security, monitoring, performance, and developer experience while contributing hands-on mobile engineering expertise.

Lead the mobile delivery roadmap, mentor engineers, and improve CI/CD practices for Android and iOS applications. Design and maintain automated build, testing, signing, and release pipelines; manage certificates, provisioning profiles, keystores, secrets, versioning, and app-store deployment. Troubleshoot mobile delivery issues while improving reliability, security, monitoring, performance, and developer experience. Collaborate with mobile engineering, QA, security, and product teams on scalable delivery practices and broader mobile initiatives.

Lead cross-functional teams delivering electronic Clinical Outcome Assessment studies from startup through closeout. Responsibilities include planning, documentation, device coordination, status reporting, timeline and budget management, risk mitigation, stakeholder communication, issue resolution, regulatory archiving, client presentations, and team mentoring. The role supports U.S. customers from India while working Eastern Time Zone hours.

Processes and validates reader invoices for medical imaging and clinical trial services. Reconciles activity data across operational and financial systems, investigates discrepancies, supports accrual reporting, maintains audit-ready documentation, and coordinates with readers, Finance, Accounts Payable, Project Management, and Reader Operations. The role also monitors workflows, produces operational reports, supports compliance, and contributes to process improvements and SOP development.

Leads complex global eCOA clinical studies from planning through closeout, managing timelines, budgets, risks, documentation, devices, quality, and client relationships. Provides operational oversight, mentorship, coaching, and development for Project Management team members. Partners with sponsors and cross-functional teams, supports clinical trial technology implementations, handles forecasting and invoicing, presents services, resolves escalations, and drives process improvements and strategic initiatives.

Validate eCOA study software and lead testing across multiple projects, including CSV deliverables, test strategy, execution (functional, integration, regression, performance, UAT), defect management, environment setup, audit-ready documentation, stakeholder communication, process improvements, and mentoring junior team members in a regulated clinical research environment.

Validate eCOA study software and maintain CSV documentation. Design, execute, and document functional, integration, regression, and performance tests. Track defects, support remediation and retesting, manage test environments and tools, and ensure regulatory audit readiness while collaborating with cross-functional and global teams.

Collaborate with multidisciplinary teams on PET and SPECT imaging studies, process imaging data, and support clinical trials and scientific publications.

Lead verification and validation activities for clinical study software, review and approve CSV/test documentation, design and execute functional/integration/regression/performance tests, manage defects and test environments, coordinate test efforts across teams (including offshore), support audits and regulatory requests, and mentor team members to improve testing processes and quality.

Create pricing estimates and change order proposals, work with project management and sales teams, maintain budget information, and support proposal processes.

Design, develop, test, and maintain scalable web applications and Microsoft Power Platform solutions. Integrate Power Apps with .NET services, implement database schemas with Entity Framework and SQL Server, participate in agile ceremonies, mentor junior developers, and collaborate with product and design stakeholders to meet business requirements.

As Director of R&D Software Engineering, oversee software development in a regulated healthcare context, ensuring compliance and quality while managing multiple development teams and delivering new initiatives.

Leads project management operations for digital physiology and clinical research programs. Responsibilities include implementing departmental strategies, managing project delivery, mentoring and developing teams, monitoring performance metrics, ensuring SOP and quality compliance, resolving customer escalations, supporting hiring and onboarding, improving processes, forecasting resources, and collaborating with cross-functional and external stakeholders. The role also participates in customer meetings and supports operational initiatives.

Lead respiratory clinical study execution from planning through closeout. Coordinate clients, vendors, sites, and internal teams; manage timelines, budgets, documentation, equipment, risks, reporting, and regulatory archiving. Maintain customer relationships, resolve escalations, support meetings and business development, and contribute to onboarding, training, and continuous improvement initiatives.

Designs and facilitates instructor-led, virtual, blended, and in-person training programs for employees and leaders. Develops learning materials, conducts needs assessments, partners with HR and business stakeholders, manages multiple learning initiatives, and evaluates program effectiveness using feedback and metrics. Supports LMS administration and contributes to leadership development, organizational capability building, and talent development strategy.

Build rapid Generative AI prototypes, mockups, interactive demos, and lightweight automation tools. Translate structured business inputs into dashboards, roadmaps, and presentations; evaluate AI tools and prompting techniques; support ideation sessions; demonstrate solutions to stakeholders; and promote AI adoption across cross-functional teams.

Lead global R&D to define technical strategy and roadmaps, prioritize AI-driven modernization, manage engineering and test teams, oversee AI/ML model validation in regulated clinical environments, own R&D budgeting and vendor partnerships, ensure regulatory compliance, and drive operational excellence and ethical AI adoption to improve clinical trial outcomes.

Lead planning, setup, monitoring, and closeout of clinical studies to ensure on‑time, in‑scope delivery. Translate client requirements, manage study documentation, equipment logistics, timelines, budgets, risks, and stakeholder communications. Resolve client issues, represent study services in meetings, and support onboarding and training of new PM team members.