The Solutions Design Analyst coordinates the eCOA design process by reviewing clinical trial protocols and translating client requirements into optimized design specifications. They collaborate with cross-functional teams to ensure accurate project delivery and present designs during milestone meetings.
You will lead the delivery of clinical trial projects from start-up through closeout, ensuring quality, timelines, and financial oversight. You will also manage stakeholder communications and support cross-functional teams to ensure protocol compliance and project success.
The Digital Product Manager will own the vision, strategy, and roadmap for the enterprise Agentic AI Platform, driving its adoption and scaling from pilot to company-wide use. They will collaborate with cross-functional teams to translate stakeholder requirements into actionable product initiatives while ensuring measurable business value and compliance.
The Assistant Clinical Project Manager supports study execution by coordinating cross-functional activities and managing project administration tasks such as billing and forecasting. They also ensure software configurations align with operational workflows while maintaining quality standards in accordance with GCP and FDA guidelines.
The Project Manager will lead respiratory clinical studies from startup through closeout, ensuring high-quality delivery within budget and timelines. They will manage study documentation, financial oversight, and cross-functional team coordination while maintaining proactive communication with sponsors.
Oversee delivery health across assigned client portfolios, coordinating clinical studies, monitoring timelines and performance, and managing risks and escalations. Build client partnerships and work with project, operational, business development, and client success teams to support governance, consistent delivery, retention, and account 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, enforce coding standards, and manage the end-to-end mobile application lifecycle.
The Clinical Data Management Associate II is responsible for reviewing, validating, and managing clinical trial data from imaging studies to ensure accuracy and integrity. They collaborate with cross-functional teams to support study setup, maintain data specifications, and resolve data discrepancies throughout the study lifecycle.
Coordinate translation projects for electronic clinical trial solutions by managing timelines, budgets, and deliverables. Communicate effectively with clients, vendors, and cross-functional teams to ensure high-quality project outcomes and regulatory compliance.
Lead and manage clinical projects from start-up to close-out, ensuring high-quality execution and adherence to timelines. Oversee project resources, financial budgeting, and regulatory compliance while coordinating with internal and external stakeholders.
The Clinical Project Manager will lead cross-functional teams in the execution of clinical trials, overseeing study startup, project planning, and closeout activities. They are responsible for maintaining high standards of quality and compliance while managing project finances and resources.
Lead global R&D strategy, teams, budgets, and roadmaps, prioritizing AI-driven modernization and the development of AI-enabled clinical trial platforms. Maintain platform quality and regulatory compliance while managing delivery, customer escalations, strategic technology partnerships, and reporting on risks and initiative outcomes.
Develop and maintain scalable Python applications, REST APIs, and data pipelines for clinical research, using cloud services and SQL databases. Collaborate with data and engineering teams to improve software quality and ensure solutions meet clinical data standards and regulatory expectations.
Coordinate the overall solutions design process for client studies by reviewing clinical trial protocols and translating requirements into optimized eCOA designs. Collaborate with cross-functional teams to ensure accurate project delivery, maintain design specifications, and support testing and change control processes.
Define and oversee end-to-end solution architectures while translating business requirements into scalable technical designs. Collaborate with cross-functional teams to evaluate technology options and guide solutions throughout the development lifecycle.
The Senior Manager will lead strategic initiatives in software quality engineering, establishing process and technology standards for eCOA projects. They are responsible for managing offshore testing vendors, driving test automation and AI integration, and ensuring all validation efforts meet regulatory and quality standards.
Lead clinical trial projects from start-up through close-out while managing timelines, resources, and project deliverables. Partner with cross-functional teams and sponsors to translate study requirements into effective project plans and solutions.
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 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.
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.
