Lead – Clinical Data Processor
Location: Bangalore, India | Remote (India)
Employment Type: Full Time
Job Requisition ID: R16935
Industry: Clinical Trials | Clinical Data Management | Specialty Solutions
Clario is a global leader in clinical trial endpoint technology, delivering innovative solutions that ensure the highest standards of data quality and operational excellence across the clinical research lifecycle. Our mission is to transform lives by generating reliable evidence that accelerates the development of life-changing therapies.
Clario is seeking a Lead, Clinical Data Processor to manage and mentor a team responsible for source document processing, query management, quality control, and workflow completion across multiple active clinical trials. The role ensures compliance with GxP standards, study protocols, and sponsor requirements while supporting critical project timelines and driving operational efficiency.
This is a strategic position for candidates with 3+ years of experience in clinical trials or healthcare operations, with at least 1 year in clinical trial-specific roles, who are ready to lead teams in a fast-paced, high-quality environment.
Lead a team performing source document processing, redaction, quality checks, and workflow execution across multiple clinical studies
Monitor, balance, and optimize team workload, ensuring timely and accurate task completion
Manage multi-staff assignments while maintaining communication with Project Managers and sponsors
Mentor and guide team members on study deliverables, processes, timelines, and SOP adherence
Apply study-specific redaction guidance, QC requirements, and GxP expectations consistently
Provision and manage customer user accounts in compliance with access standards
Review image, video, and document quality; perform redaction, source preparation, translation, or DICOM linking as needed
Issue queries, follow up with study sites, and escalate risks or trends to Project and Operations Managers
Support generation and distribution of final study closeout deliverables
Ensure all activities align with internal SOPs, project-specific instructions, and regulatory standards
Participate in SOP updates, Quick Reference Guides, and work instruction development
Facilitate cross-functional communication between Project Support, QA, and other departments
Support sponsor audits, quality assurance reviews, and follow-up actions
Associate or Bachelor’s degree in Computer Science, IT, Life Sciences, or related field, or equivalent experience
3+ years of experience in clinical trials, healthcare, or clinical data management; minimum 1 year in clinical trial-specific roles preferred
Proficiency in MS Office tools (Word, Excel, Teams, OneNote)
Strong understanding of PII/PHI compliance, redaction, and Good Documentation Practice (GDocP)
Demonstrated leadership experience in supervising or mentoring teams
Exceptional attention to detail and accuracy in data processing
Strong organisational, prioritisation, and problem-solving capabilities
Ability to work independently and collaboratively under pressure
Excellent interpersonal, written, and verbal communication skills
Professionalism, accountability, and commitment to quality
Fluent in English, both written and verbal
Clario offers competitive pay, incentives, provident fund, medical insurance, and flexible hybrid work arrangements. You will work in a collaborative, globally connected environment with opportunities to influence clinical research operations and improve patient outcomes.
At Clario, your contributions help bring life-changing therapies to patients faster while supporting innovation in clinical science, technology, and operational excellence.
Apply now on ThePharmaDaily.com to advance your career as a Lead, Clinical Data Processor and join a global leader in clinical trial technology.a
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