Lead, Clinical Data Processor
Location: Bangalore, India (On-site / Hybrid) | India (Remote Options Available)
Job Type: Full-Time
Job Requisition ID: R16935
Experience Required: 3–6 Years
Industry: Clinical Research | Clinical Trials | Healthcare Technology
About the Company
Clario is a global leader in clinical trial endpoint technology, delivering high-quality data and evidence to accelerate drug development. With a strong focus on innovation, compliance, and operational excellence, Clario partners with global sponsors to support life-changing therapies and improve patient outcomes worldwide.
Job Overview
Clario is seeking an experienced Lead, Clinical Data Processor to manage and guide clinical data processing activities across multiple active clinical trials within its Specialty Solutions division. This leadership role is responsible for overseeing source document processing, query management, quality control, and workflow completion while ensuring compliance with regulatory and sponsor requirements.
The ideal candidate will demonstrate strong people management skills, attention to detail, and the ability to maintain data accuracy, timelines, and quality standards in a fast-paced clinical research environment.
Key Responsibilities
Lead and oversee source document processing activities in accordance with study-specific redaction guidelines, QC standards, and GxP requirements
Provision and manage customer user access across assigned clinical studies in compliance with access control policies
Execute and monitor workflow events to ensure timely and accurate study execution
Review image, video, and document quality; perform redaction and source preparation activities
Coordinate translation services and DICOM link creation when required
Issue and track study queries; perform routine follow-ups with clinical sites
Identify trends, risks, or quality issues and escalate to Project Managers and Operations leadership
Support generation and distribution of final study close-out deliverables
Monitor team workload and productivity; ensure balanced task allocation and adherence to timelines
Oversee large, multi-resource tasks while maintaining quality and stakeholder communication
Support internal and external communications regarding delays, issues, or risks
Collaborate with supervisors to maintain SOPs aligned with regulatory, client, and internal standards
Lead or participate in project and team meetings; guide staff on processes, deliverables, and timelines
Support Quality Assurance activities, including sponsor audits and corrective actions
Partner with cross-functional teams to enhance tools, procedures, and training programs
Ensure adherence to SOPs, work instructions, and study documentation
Contribute to SOP updates, Quick Reference Guides, and Work Instruction development
Maintain up-to-date industry, regulatory, and technical knowledge through continuous learning
Required Qualifications & Skills
Associate or Bachelor’s degree in Computer Science, Information Technology, Life Sciences, or a related discipline (or equivalent practical experience)
3–6 years of experience in clinical trials, healthcare, or a related regulated environment
Minimum 1 year of hands-on clinical trial experience preferred
Strong proficiency in Microsoft Office tools, including Word, Excel, Teams, and OneNote
Demonstrated ability to identify PII/PHI deviations and apply Good Documentation Practices (GDP) for redaction
Exceptional attention to detail with a strong focus on data accuracy and quality
Ability to work independently and collaboratively under tight timelines
Strong organisational, prioritisation, and problem-solving skills
Excellent written and verbal communication skills in English
Professional, accountable, and quality-driven mindset
Ability to work from Bangalore (on-site or hybrid) or remotely within India
What Clario Offers
Competitive salary and performance-based incentives
Provident Fund and comprehensive medical insurance
Employee engagement programs and local events
Modern office infrastructure with flexible remote work options
Career growth opportunities in a global clinical research organization
Why Join Clario
At Clario, the mission is to transform lives by unlocking better clinical evidence. Every role contributes to accelerating access to innovative therapies for patients worldwide. Whether in clinical operations, technology, or support functions, employees are empowered to make a meaningful impact while growing their careers in a collaborative and purpose-driven environment.
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