Clinical Data Processor, Specialty Solutions

eResearch Technology; Bengaluru; Remote; INR 420,000 - 640,000; Full time

Benefits offered by this job

Competitive pay

Shift allowances

Provident fund

Medical insurance

Remote work flexibility

Employee programs

Job summary

Clario, part of Thermo Fisher Scientific, is seeking a Clinical Data Processor to support source documentation accuracy across global studies. You will handle study workflows, redact sensitive records, and manage user access for assigned trials.

The role requires 10 months to 1 year in clinical trials or related domains, strong MS Office skills, and excellent attention to privacy and GDP practices. Remote work flexibility is offered with international time-zone shifts.

Qualifications

• High school diploma or Associate/Bachelor's degree in CS/IT or related field.
• 10 months to 1 year of experience in clinical trials, healthcare or related domain.
• 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.

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.

Skills

English fluency

PII/PHI handling

Independent working

Education

Bachelor's degree

Associate degree

Tools

MS Office

Job description

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.

What We Offer

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

What You'll Be Doing

• 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

What 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

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.