Clario, part of Thermo Fisher Scientific, is hiring for the position of Clinical Data Processor – Specialty Solutions in Bangalore, India, and India Remote. This is a full-time opportunity for candidates interested in clinical trials, healthcare documentation, clinical data processing, and clinical research operations.
The selected candidates will support clinical trial workflows by reviewing and redacting source documents, processing images and videos, identifying personally identifiable information (PII) and protected health information (PHI), and ensuring documentation accuracy and compliance.
Job Details
| Particulars | Details |
|---|---|
| Company | Clario (Part of Thermo Fisher Scientific) |
| Job Role | Clinical Data Processor |
| Team | Specialty Solutions |
| Job ID | R16784 |
| Job Location | Bangalore, India / India Remote |
| Job Type | Full-Time |
| Experience | 0–2 Years |
| Preferred Experience | 1+ Year |
| Qualification | High School Diploma, Associate Degree or Bachelor’s Degree |
| Work Mode | Bangalore / Remote |
| Shift | European or US Time Zone Shifts |
| Job Posting | November 2, 2026 |
Positions Available
Clinical Data Processor – Specialty Solutions
The role involves processing clinical trial source documentation, managing study-specific workflows, reviewing images and documents, and supporting clinical study closeout activities.
Key Responsibilities
- Execute study-specific workflows, including creation, resumption, cancellation, and completion of Workflow Runs.
- Review and redact images, videos, and documents according to study requirements and timelines.
- Provision customer user accounts for assigned clinical studies and trials.
- Coordinate source document translations and create DICOM image links when required.
- Use SightHound and PDF redaction software to process source documents.
- Raise queries and follow up with clinical study sites to resolve documentation issues.
- Support the preparation and distribution of final study closeout deliverables.
- Collaborate with cross-functional teams to ensure appropriate tool usage and compliance with study specifications.
- Participate in project and team meetings to discuss study progress and expectations.
- Maintain quality, professionalism, and accountability in assigned deliverables.
Eligibility Criteria and Qualifications
Candidates applying for the Clinical Data Processor position at Clario should meet the following requirements:
- High school diploma, Associate Degree, or Bachelor’s Degree in Computer Science, Information Technology, or a related field.
- 0–2 years of experience in clinical trials, healthcare, or a related domain.
- At least 1 year of experience is preferred.
- Fluency in written and spoken English.
- Willingness to work European or US time zone shifts.
Required Skills
Candidates should have the following skills:
- Strong proficiency in Microsoft Office applications, including Word, Excel, Teams, and OneNote.
- Ability to identify Personally Identifiable Information (PII) and Protected Health Information (PHI).
- Knowledge of Good Documentation Practices (GDP).
- Document review and redaction skills.
- Attention to detail and accuracy.
- Ability to work independently and collaboratively.
- Familiarity with clinical trial documentation workflows.
Salary and Benefits
Clario offers the following benefits for this position:
- Competitive pay.
- Shift allowances and incentives.
- Provident Fund (PF).
- Medical insurance.
- Employee engagement programs and local events.
- Modern office spaces.
- Remote work flexibility.
