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Clinical Data Processor, Specialty Solutions

Clarioclinical

Skills

Required

  • clinical trials
  • MS Office tools
  • PII/PHI

Preferred

  • Execute study-specific workflows
  • source document translation
  • create DICOM image links
  • SightHound
  • PDF redaction software
  • Issue queries

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.

About Clarioclinical

  • 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.

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
  • 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

Requirements

  • 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

Benefits

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