Clinical Data Processor, Specialty Solutions
- Remote · India
- Remote
- Mid Level
- 1+ years
- Associate degree
- Posted
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
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