R&D Solution Architect
Clairo
R&D Solution Architect
Clairo
Clinical trial endpoint technologies and management
At Clario, part of Thermo Fisher Scientific, we develop regulated technology that helps unlock better evidence and improve patient outcomes worldwide. Our software platforms support clinical trials, diagnostics, and medical decision‑making in highly controlled regulatory environments.
As an R&D Solution Architect, you will shape the technical vision and architecture of innovative solutions that support our clinical technology platforms. Working closely with R&D, Product Management, engineering teams, and business stakeholders, you will translate complex requirements into secure, scalable, and reliable solutions aligned with our enterprise architecture. From initial concept through implementation, you will guide architectural decisions, influence technology strategy, and help deliver solutions that make a meaningful difference. Join us and help advance the technology behind better clinical evidence.
At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.
Clario is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
Clario provides clinical trial endpoint technologies, including software, connected devices, and artificial intelligence to collect and analyze data across cardiac safety, eCOA, medical imaging, precision motion, and respiratory endpoints. Its platform supports site-based, hybrid, and fully decentralized trials, gathering data from devices, questionnaires, and imaging, then processing and analyzing it to produce reliable clinical evidence, with integrated training and 24/7 support. The company differentiates itself with a broad end-to-end suite plus deep regulatory expertise and a global deployment network that enables rapid localization in 100+ languages. Its goal is to simplify the clinical trial process while improving patient safety and retention, promoting patient choice and diversity, and advancing health equity by prioritizing both physical and mental well-being.
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