Lead, Clinical Data Processor | Bangalore, India (Onsite/Hybrid)
Location: Bangalore, India (Remote options available within India)
Job Type: Full-Time
Experience Level: Mid to Senior – 3+ Years
Category: Clinical Data Management / Specialty Solutions
Job ID: R16935
About the Role
Clario, a global leader in clinical trial endpoint technology, is seeking a Lead, Clinical Data Processor to oversee the processing and quality management of source documents across multiple active clinical trials. This leadership role ensures operational excellence, accuracy, and compliance while guiding a team responsible for workflow completion, query management, and quality checks within our Specialty Solutions division.
As a key member of the Project Support team, you will interact with project managers, study sites, and internal stakeholders to maintain high standards of clinical data quality and timely deliverables.
Key Responsibilities
Lead a team in source document processing, redaction, and quality control, ensuring compliance with study-specific guidance, GxP expectations, and regulatory standards.
Provision and manage customer user accounts across assigned studies while maintaining access compliance.
Oversee workflow events related to study execution, ensuring accuracy and timely completion.
Review image, video, and document quality; facilitate translation, DICOM link creation, and redaction as required.
Issue and manage queries; conduct follow-ups with study sites and escalate trends or risks to Project and Operations Managers.
Monitor and balance team workload, driving process improvements for efficiency and accuracy.
Support project closeout by generating and distributing final deliverables.
Collaborate with QA and Project Management teams during audits, follow-up actions, and cross-functional initiatives.
Mentor team members, lead project meetings, and maintain adherence to SOPs, work instructions, and study-specific documentation.
Maintain professional, accountable, and high-quality deliverables across all assignments.
Qualifications & Experience Required
Associate’s or Bachelor’s degree in Computer Science, IT, Life Sciences, or related field (or equivalent professional experience).
Minimum 3+ years in clinical trials, healthcare, or related fields; 1+ year of clinical trial experience preferred.
Proficiency in MS Office Suite: Word, Excel, Teams, OneNote.
Strong understanding of Good Documentation Practice (GDP) and ability to identify PII/PHI deviations.
Exceptional attention to detail, organizational skills, and problem-solving capabilities.
Ability to work independently and collaboratively under pressure while demonstrating sound judgment.
Excellent verbal and written communication skills in English.
Based in or able to work from Bangalore, India (onsite or hybrid).
What We Offer
Competitive compensation and performance incentives.
Provident Fund, medical insurance, and comprehensive employee benefits.
Flexible hybrid work options and modern office spaces.
Engaging employee programs, local events, and professional development opportunities.
Why Join Clario?
Clario’s mission is to transform lives by unlocking better evidence in clinical trials. In this role, you will lead a team contributing directly to high-quality clinical research and faster delivery of life-changing therapies to patients globally.
How to Apply
Submit your application via thepharmadaily.com to join Clario’s global team advancing clinical data quality and operational excellence.
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