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Clinical Data Processor, Specialty Solutions

Role overview

Summary

The Clinical Data Processor role at Clario supports the integrity and efficiency of clinical trials by ensuring the accuracy and compliance of source documentation. This position is part of the Specialty Solutions team, which focuses on generating better evidence across global studies.

Qualifications

  • High school diploma or Associate/Bachelor’s degree in computer science, information technology, or related field.
  • Proven expertise in MS Office tools including Word, Excel, Teams, and OneNote.
  • Strong proficiency in identifying PII/PHI and applying Good Documentation Practices.
  • Fluency in English (written and verbal).
  • Preferred: 10 months–1 year of experience in clinical trials, healthcare, or a related domain; 1+ year

Responsibilities

  • 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

Key facts

Hard skills

Other skills

  • Microsoft Office
  • Technical Acumen
  • Detail Oriented
  • Teamwork
  • Communication
  • Accountability
  • Collaboration

About the company

Clario logo

Clario

  • Clinical Research (CRO)
  • XLarge
  • 1,001–5,000
Clario is a leading healthcare research and technology company that generates high quality clinical evidence for our pharmaceutical, biotech, and medical device partners. We offer comprehensive evidence generation solutions that combine eCOA, cardiac safety, medical imaging, precision motion, and respiratory endpoints. Since our founding more than 50 years ago, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported clinical trials over 26,000 times in more than 100 countries. Our global team of science, technology, and operational experts have supported over 60% of all FDA drug approvals since 2019. For more information, visit Clario.com

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Job description

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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