The Project Manager will lead study planning, setup, monitoring, and closeout activities for eCOA projects while ensuring quality, timeline, and budget objectives are met. They will also coordinate with cross-functional teams, manage study documentation, and serve as the primary point of contact for operational readiness.
Lead clinical trial projects from planning and setup through monitoring and closeout, ensuring delivery on time, within budget, and to quality standards. Coordinate clients, internal teams, and external partners; manage study documentation, equipment, reporting, risks, milestones, and customer issues.
The Project Manager will coordinate the end-to-end delivery of eCOA solutions, ensuring projects meet quality, budget, and timeline requirements. They will serve as the primary point of contact for clients, managing requirements, risks, and cross-functional team collaboration throughout the study lifecycle.
The manager will develop, coordinate, and maintain clinician training and calibration programs while monitoring clinical performance to ensure quality standards are met. They will also lead training sessions, provide clinical consultation, and implement SOPs to ensure compliance with GCP requirements.
The Senior Enterprise Architect will define the enterprise data architecture blueprint and set technology standards for ingestion, storage, and transformation. They will also lead data maturity initiatives and collaborate with engineering teams to ensure robust data governance and security.
You will lead the architectural design and development of the Clario mobile platform using .NET MAUI, C#, and MVVM patterns. Additionally, you will mentor engineering teams, enforce coding standards, and manage the end-to-end mobile application lifecycle including CI/CD and deployment.
The Project Manager will lead the planning, execution, and closeout of respiratory clinical studies while serving as the primary point of contact for clients. They are responsible for managing study timelines, budgets, and cross-functional team collaboration to ensure high-quality delivery of clinical trial services.
The Project Coordinator supports clinical study teams by managing documentation, database maintenance, and equipment tracking throughout the study lifecycle. They also facilitate financial reconciliation, report generation, and issue management to ensure operational excellence and customer satisfaction.
The Account Director will lead strategic client accounts, serving as the primary point of contact to drive satisfaction, retention, and growth. They will collaborate with internal teams to ensure operational excellence and align client objectives with Clario's products and services.
Interpret and review oncology clinical data and imaging endpoints, complete study documentation, and ensure work meets protocol, Good Clinical Practice, and quality requirements. Collaborate with internal teams, sponsors, and regulatory stakeholders; support training, audits, issue resolution, and continuous improvement.
Drive profitable business growth by supporting pricing and margin initiatives, optimizing customer solutions, and contributing to strategic commercial opportunities. Lead change management and process improvement initiatives, analyze performance and business data, and ensure implementations align with operational, compliance, and risk requirements.
Design and maintain scalable, data-driven software solutions and robust data pipelines for clinical research. Collaborate with cross-functional teams to build REST APIs and ensure compliance with industry standards like GCP and FDA expectations.
The Lead Customer Service Experience Manager will oversee complex customer escalations and develop resolution strategies to improve departmental processes. They will also mentor team members and collaborate with internal stakeholders to provide risk assessments and actionable data-driven recommendations.
The Account Director will generate new business opportunities and manage a sales pipeline to achieve revenue targets within the medical imaging and clinical research sector. They will also lead proposal development, negotiate contracts, and maintain strategic relationships with clients.
The Associate Product Manager will support product strategy, roadmap development, and lifecycle management for software, devices, and services. They will collaborate with cross-functional teams to translate market needs into product requirements and coordinate successful product launches.
Lead the development, maintenance, and continuous improvement of high-quality technical documentation across the software portfolio. Collaborate with cross-functional teams to translate complex technical concepts into clear, user-friendly content for end-users.
Coordinate site and operational activities throughout the clinical imaging study lifecycle, including study start-up and data management. Perform image quality control, resolve data discrepancies, and maintain accurate study documentation in accordance with protocols.
The Project Manager will lead cross-functional teams through the planning, execution, and closeout of global eCOA clinical studies. They are responsible for managing project timelines, budgets, and stakeholder expectations while ensuring high-quality delivery and regulatory compliance.
The Senior Lead, Clinical Project Manager provides leadership and governance for global clinical research projects to ensure they are delivered on time, within budget, and with high quality. They are responsible for managing staff, overseeing project execution, and driving operational excellence through process improvements and cross-functional collaboration.
The Manager, Medical Communications will lead the development of scientific communication strategies and manage the creation of publications, white papers, and presentations to support eCOA business objectives. They will act as a strategic liaison between scientific, marketing, and executive teams to translate complex clinical data into impactful narratives.
You will lead the end-to-end creation and scaling of new subscription-based products using AI-driven tools and performance marketing strategies. You are responsible for managing the P&L, optimizing the web funnel, and orchestrating the customer lifecycle through the AARRR framework.
The Project Manager will lead the end-to-end execution of cardiac safety studies, ensuring they are delivered on time, within budget, and to high quality standards. They will act as the primary operational lead, coordinating cross-functional teams, managing study documentation, and maintaining strong relationships with sponsors and clinical sites.
The Cardiac Specialist II is responsible for performing advanced ECG, Holter, and ambulatory blood pressure monitoring analyses for global clinical trials. They also support quality initiatives, mentor team members, and ensure data integrity and patient safety throughout the clinical research process.
The Principal Customer Education Specialist serves as a subject matter expert to develop and implement innovative training solutions for customers and internal stakeholders. They lead product readiness initiatives, monitor quality metrics, and collaborate with business development to drive customer success and study execution.
You will investigate data discrepancies, process correction requests, and maintain accurate study documentation within established regulatory procedures. Additionally, you will collaborate with global teams to support data reconciliation activities and ensure database updates meet sponsor timelines.
You will partner with clinical scientists to design and implement training and calibration strategies that ensure high-quality clinical endpoint assessments. Additionally, you will monitor clinician performance, provide coaching, and ensure all training documentation complies with regulatory standards.
You will lead the design and implementation of enterprise DevOps and cloud infrastructure solutions while optimizing CI/CD pipelines for secure and scalable software delivery. Additionally, you will drive automation initiatives and mentor engineering teams to elevate DevOps maturity across the organization.
Develop pricing strategies, budgets, and commercial proposals while collaborating with cross-functional teams including Sales, Finance, and Operations. Ensure high-quality documentation and compliance while supporting customer negotiations and strategic business growth.
You will lead the architectural design and development of cross-platform mobile applications using .NET MAUI and C#. Additionally, you will mentor engineering teams and oversee the full mobile application lifecycle, including CI/CD and deployment to app stores.
The Imaging Research Associate coordinates site and operational activities throughout the clinical study lifecycle to ensure high-quality data delivery. They are responsible for managing site communications, processing study data, resolving discrepancies, and supporting project managers with administrative tasks.
The Archive Specialist manages final study archives post-database lock, ensuring all clinical trial documentation is complete, organized, and compliant with regulatory standards. They coordinate with project teams to acquire documentation, perform quality audits, and manage the delivery of archive packages to sponsors and sites.
Design, develop, and maintain scalable data pipelines and software architectures to support clinical trial operations. Integrate LLM-powered solutions and ensure data quality, governance, and reliability across analytical systems.
The Cardiologist will interpret cardiac data such as ECGs and stress tests to generate endpoint data for pharmaceutical sponsors. They will also provide scientific expertise, oversee quality assurance programs, and assist in the development of cardiac safety and efficacy strategies.
You will architect and develop scalable test automation for a microservices-based platform while integrating AI to enhance test design and coverage. Additionally, you will collaborate with cross-functional teams to define test strategies, troubleshoot complex failures, and mentor junior engineers.
The Senior Cardiologist will provide scientific and medical leadership for cardiac safety, efficacy, and digital physiology solutions within clinical trials. Responsibilities include partnering with pharmaceutical sponsors, contributing to regulatory strategy, and overseeing the interpretation of cardiac data.
The Clinical Project Manager leads the planning, execution, and delivery of clinical projects while ensuring compliance with regulatory and quality standards. They manage project timelines, resources, financial activities, and cross-functional team collaboration to achieve high-quality outcomes.
Lead validation activities for study software in accordance with regulatory standards and manage the overall test effort across assigned projects. Review and approve Computer System Validation packages while partnering with cross-functional teams to ensure high-quality, compliant software deliverables.
The analyst is responsible for delivering high-quality eCOA solution designs by translating pharmaceutical client requirements and study protocols into optimized specifications. They coordinate the design process and collaborate with cross-functional teams to ensure data integrity and efficient project delivery.
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.
