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Clario, a global leader in endpoint technology for clinical trials, is hiring a Clinical Data Processor for its Specialty Solutions team. This role is ideal for freshers and early-career professionals looking to build a strong foundation in clinical data processing, source documentation review, and workflow management within modern clinical research.
If you’re detail-oriented, comfortable with technology, and passionate about contributing to high-quality clinical trial data, this opportunity provides a pathway into one of the fastest-growing sectors in healthcare.
⭐ Key Responsibilities
As a Clinical Data Processor at Clario, you will:
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- Execute study-specific workflows: creation, resumption, cancellation & completion of Workflow Runs
- Review and redact images, videos & documents according to study requirements
- Provision customer and study-site user accounts
- Support source document translation and generate DICOM image links
- Use tools like SightHound, PDF redaction software, MS Office
- Raise and resolve queries with study sites to ensure documentation accuracy
- Contribute to final study closeout deliverables
- Collaborate with cross-functional teams to ensure proper tool usage
- Uphold Good Documentation Practices (GDP) and protect PII/PHI
- Attend project/team meetings for updates and alignment
🎓 Required Qualifications
- High school diploma or Associate/Bachelor’s in Computer Science, IT, Life Sciences, or related field
- 0–2 years of experience in clinical trials, healthcare, data processing or similar domain
- Strong skills in MS Word, Excel, Teams, OneNote
- Ability to identify and redact PII/PHI accurately
- Excellent communication skills in English
- Ability to work independently and collaboratively
🎁 Benefits
- Competitive salary & incentives
- Provident fund & medical insurance
- Remote work flexibility + modern offices
- Employee engagement programs
- Opportunity to contribute to global clinical trials impacting patient lives
📌 How to Apply
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