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:

• 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

Application Link