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Clario

Clinical Data Processor, Specialty Solutions

Posted an hour ago
0-2 years experience
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AI Summary

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.


What We Offer

  • Competitive pay, shift allowances and incentives
  • Provident fund and medical insurance
  • Engaging employee programs and local events
  • Modern office spaces and remote work flexibility

What You’ll Be Doing

  • Execute study-specific workflows including creation, resumption, cancellation, and completion of Workflow Runs
  • Review and redact images, videos, and documents per study parameters and timelines
  • Provision customer user accounts for assigned studies and trials
  • Facilitate source document translation and create DICOM image links as needed
  • Use tools such as SightHound and PDF redaction software to process source documents
  • Issue queries and follow up with study sites to resolve documentation issues
  • Support generation and distribution of final study closeout deliverables
  • Collaborate with cross-functional teams to ensure proper tool usage and adherence to specifications
  • Attend project and team meetings to align on study progress and expectations
  • Maintain high standards of quality, professionalism, and accountability in all deliverables

What We Look For

  • High school diploma or Associate/Bachelor’s degree in computer science, information technology, or related field
  • 10months–1 year of experience in clinical trials, healthcare, or a related domain; 1+ year preferred
  • Proven expertise in MS Office tools including Word, Excel, Teams, and OneNote
  • Strong proficiency in identifying PII/PHI and applying Good Documentation Practices
  • Demonstrated ability to work independently and collaboratively in dynamic environments
  • Fluency in English (written and verbal)
  • Willingness to work European or US time zone shifts

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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