Lead, Clinical Data Processor
Location: Bangalore, India (Hybrid/Remote)
Job Type: Full-Time
Job Requisition ID: R16935
Experience Required: Minimum 3 Years
About the Role
Clario, a global leader in clinical trial endpoint technology, is seeking a Lead, Clinical Data Processor to join our Specialty Solutions division. In this leadership role, you will manage and guide a team responsible for the accurate and timely processing of clinical trial data, including source document processing, query management, quality checks, and workflow completion across multiple active studies. Your leadership will ensure the highest standards of data integrity, compliance, and operational excellence, supporting critical global project timelines and maintaining close collaboration with internal and external stakeholders.
This is an excellent opportunity for experienced professionals with a background in clinical trials and data processing to drive quality assurance efforts and enhance operational workflows within a globally recognized company.
Key Responsibilities
Ensure adherence to study-specific redaction guidelines, quality control (QC) requirements, and GxP expectations for source document processing.
Oversee customer user account provisioning for assigned studies, ensuring compliance with access requirements and maintaining security protocols.
Manage and perform workflow events related to study execution, ensuring both accuracy and timeliness of deliverables.
Review image, video, and document quality; perform redaction and source preparation; facilitate translation or DICOM link creation when required.
Issue queries and conduct follow-ups with study sites; escalate emerging trends or risks to Project and Operations Managers.
Support final study closeout deliverables, ensuring timely and accurate completion.
Monitor and balance team workload, driving improvements to enhance task completion accuracy and efficiency.
Lead large-scale, multi-staff tasks, ensuring alignment with project goals and effective communication with Project Managers or customers.
Communicate any delays, issues, or risks to internal or external stakeholders in a timely and transparent manner.
Collaborate with supervisors and cross-functional teams to maintain and update procedures that meet internal, client, and regulatory requirements.
Lead or participate in project/team meetings, providing guidance on deliverables, processes, and timelines.
Support Quality Assurance teams during sponsor audits and assist with follow-up actions.
Partner with other departments to develop tools, procedures, and training materials aimed at strengthening the Project Support team’s effectiveness.
Ensure the smooth execution of projects by facilitating cross-functional collaboration and communication.
Manage expectations and project timelines effectively with both Clario Project Management and external clients.
Maintain strong professionalism, accountability, and quality in all deliverables.
Ensure fluency and consistency in English-language communications, both written and verbal.
Adhere to SOPs, project-specific instructions, and study documentation, ensuring full regulatory compliance.
Contribute to the development of SOP updates, team QRGs, and Work Instruction materials.
Engage in continuous training and learning to maintain technical proficiency and industry knowledge.
Required Qualifications
Education: Associate/Bachelor’s degree in Computer Science, IT, Life Sciences, or a related field (or equivalent practical experience).
Experience: Minimum 3 years of experience in clinical trials, healthcare, or a related field, with at least 1 year of clinical trial experience preferred.
Technical Skills: Proficiency with MS Office tools (Word, Excel, Teams, OneNote).
Knowledge: Understanding of PII/PHI identification and Good Documentation Practices for redaction.
Attention to Detail: Exceptional accuracy and attention to detail when processing data and documents.
Collaboration Skills: Ability to work both independently and collaboratively within a team, with excellent judgment under pressure.
Organizational Skills: Strong organizational, prioritization, and problem-solving capabilities to manage multiple tasks efficiently.
Communication Skills: Excellent interpersonal, written, and verbal communication abilities, maintaining professionalism in all interactions.
Work Environment: Based in or able to work from Bangalore in a hybrid or remote capacity.
Compensation & Benefits
Competitive salary with performance-based incentives.
Provident Fund and comprehensive medical insurance.
Access to employee engagement programs and local events.
Hybrid work flexibility with modern office spaces.
Why Join Clario?
At Clario, we are driven by a singular purpose: transforming lives by unlocking better evidence. We empower our global teams to make meaningful impacts every day, whether advancing clinical science, developing innovative technology, or supporting critical projects for life-changing therapies. As a Lead, Clinical Data Processor, you will play a key role in improving the quality and speed of clinical trials, directly contributing to the faster delivery of treatments to patients worldwide.
If you are passionate about data integrity, leadership, and making a real-world impact, we encourage you to apply and join our dynamic, global team.
For more career opportunities in the clinical research and healthcare sector, visit ThePharmaDaily.com.
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