Principal Technical Writer
Clairo
Principal Technical Writer
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.
We are seeking a Principal Technical Writer to join our Technical Product Development team and lead the creation, management, and continuous improvement of high-quality technical documentation across our product portfolio. In this role, you will collaborate with engineering, product management, and cross-functional teams to translate complex technical information into clear, accessible content that enhances the user experience. If you are passionate about technical communication, documentation excellence, and driving consistency across innovative software products, we encourage you to apply.
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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