Lead, Clinical Data Processor

Bangalore, IndiaHybrid

Responsibilities

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.
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

experience in clinical trials, healthcare, or a related field; 1+ year clinical trial
experience preferred Proficiency with MS Office tools (Word, Excel, Teams, OneNote) Ability to identify PII/PHI deviations and apply Good Documentation Practice for redaction Exceptional attention to detail and accuracy Ability to work independently and collaboratively, with strong judgement under pressure Strong organisational, prioritisation, and problem‑solving skills Excellent interpersonal, written, and verbal communication abilities Ability to maintain professionalism and a positive attitude at all

What We Offer Competitive pay 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 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

Join us a global leader in clinical trial endpoint technology and help ensure the highest standards of data quality throughout our clinical study workflows.