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The role involves executing study-specific workflows, including the creation and completion of workflow runs, and reviewing/redacting sensitive clinical documentation. You will also facilitate source document translation, manage user accounts, and collaborate with cross-functional teams to ensure data integrity and project timelines.
At Clario, part of Thermo Fisher Scientific. Join us as a Clinical Data Processor in our Specialty Solutions team, where your work will directly support the integrity and efficiency of clinical trials that bring life-changing therapies to patients faster. In this role, you’ll help ensure the accuracy and compliance of source documentation, enabling better evidence generation across global studies. If you’re detail-oriented, tech-savvy, and passionate about improving healthcare outcomes, we’d love to hear from you.
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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.
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