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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.
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 a Data Coordinator I within our Clinical Data Management team, you’ll help ensure clinical study data is accurate, complete, and moving efficiently through our processes. You’ll investigate data discrepancies, process data correction requests, and maintain organized study documentation while working within established procedures and timelines. This is an entry-level opportunity for someone who enjoys solving problems, working with data, and learning in a collaborative global environment. You’ll receive comprehensive, hands-on training and gain exposure to different studies, sponsors, and teams as you build your career in clinical data management.
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.
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