At Clario, part of Thermo Fisher Scientific. Join us a global leader in clinical
trial endpoint technology and help ensure the highest standards of data quality
throughout our clinical study workflows. As Lead, Clinical Data Processor, you
will lead a team responsible for source document processing, query management,
quality checks, and workflow completion across multiple active clinical trials
within our Specialty Solutions division. Your leadership will ensure accuracy,
compliance, and operational excellence while supporting critical project
timelines for global sponsors.

What We Offer
Competitive pay and incentives
Provident Fund and medical insurance
Engaging employee programs and local events
Up-to-date office spaces and work from home flexibility

What You’ll Be Doing
Understand and apply study‑specific redaction guidance, QC requirements, and
GxP expectations for source document processing
Provision customer user accounts across assigned studies and ensure
compliance with access requirements




Manage and perform workflow events related to study execution, ensuring
accuracy and timeliness
Review image, video, and document quality; perform redaction and source
preparation; facilitate translation or DICOM link creation when required
Issue queries and conduct routine follow‑up with study sites; escalate trends
or risks to Project and Operations Managers
Assist with generating and distributing final study closeout deliverables
Monitor and balance team workload; drive improvements to ensure timely and
accurate task completion
Oversee large, multi‑staff tasks, ensuring quality and communication with
Project Managers or customers
Support Project Support staff in communicating delays, issues, or risks to
internal or external stakeholders
Collaborate with supervisors to maintain procedures that meet internal,
client, and regulatory requirements
Lead or participate in project/team meetings and guide staff on deliverables,
processes,

📌 Lead, Clinical Data Processor Bengaluru
🏢 Clario
📍 Bengaluru