Clario is hiring for the position of Lead, Clinical Data Processor in India. This opportunity is suitable for professionals with an educational background in Life Sciences, Computer Science, Information Technology, or a related discipline and experience in clinical trials, healthcare, or related operations.
The Clario Lead Clinical Data Processor role focuses on clinical trial source document processing, data quality, query management, redaction, workflow execution, and team coordination. The selected professional will support multiple active clinical studies and help ensure that clinical trial data and source documentation are processed accurately and in accordance with study requirements, SOPs, GxP expectations, and applicable quality standards.
Clario, part of Thermo Fisher Scientific, provides endpoint technology and evidence-generation solutions for clinical trials across areas including medical imaging, eCOA, cardiac, respiratory, and precision motion.
Key Responsibilities
As a Lead Clinical Data Processor at Clario, your responsibilities will include:
- Apply study-specific redaction guidance, QC requirements, and GxP expectations during source document processing.
- Manage and execute workflow activities associated with clinical study operations.
- Review the quality of clinical trial images, videos, documents, and other source materials.
- Perform document redaction and source preparation while maintaining data quality and confidentiality.
- Facilitate translation activities or DICOM link creation when required.
- Provision customer user accounts for assigned clinical studies and ensure appropriate access.
- Raise queries and conduct routine follow-up with clinical trial sites.
- Escalate recurring issues, risks, or trends to Project and Operations Managers.
- Support preparation and distribution of final clinical study closeout deliverables.
- Monitor and balance team workloads to ensure timely completion of activities.
- Oversee large tasks involving multiple team members while maintaining quality standards.
- Communicate project delays, operational issues, and risks to relevant stakeholders.
- Collaborate with supervisors to maintain procedures aligned with internal, sponsor, and regulatory requirements.
- Participate in project and team meetings and provide guidance regarding processes, timelines, and deliverables.
- Support Quality Assurance teams during sponsor audits and subsequent follow-up activities.
- Contribute to the development of operational tools, procedures, and training materials.
- Follow SOPs, project-specific instructions, study documentation, and Good Documentation Practice.
- Participate in SOP updates, Quick Reference Guides (QRGs), and Work Instruction development.
Qualification and Eligibility
Candidates interested in the Clario Clinical Data Processor job should meet the following requirements:
- Associate or Bachelor’s degree in Life Sciences, Computer Science, Information Technology, or a related field, or equivalent relevant experience.
- 3+ years of experience in clinical trials, healthcare, or a related field.
- At least 1 year of clinical trial experience is preferred.
- Proficiency with Microsoft Office applications, including Excel, Word, Teams, and OneNote.
- Understanding of PII/PHI and the ability to identify deviations involving sensitive information.
- Knowledge of Good Documentation Practice and document redaction.
- Excellent attention to detail and commitment to data accuracy.
- Strong organisational and prioritisation abilities.
- Good analytical, judgement, and problem-solving skills.
- Ability to work independently as well as within cross-functional teams.
- Strong written and verbal English communication skills.
Which Degrees Can Apply?
Based on Clario’s stated educational requirements, candidates from backgrounds such as B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Computer Science, Information Technology, and other relevant disciplines may be suitable, provided they meet the role’s experience and skill requirements.
Skills Required
Candidates applying for the Lead Clinical Data Processor position should have skills or exposure in:
- Clinical trial operations
- Clinical data/source document processing
- Query management and site follow-up
- Quality control and data accuracy
- Source document redaction
- PII/PHI identification
- Good Documentation Practice
- GxP requirements
- SOP and Work Instruction compliance
- Microsoft Excel and Word
- Clinical study workflow management
- Stakeholder communication
- Team workload management
- Problem-solving and prioritisation
Is This a Clinical Data Management Role?
This position is related to clinical data operations but is not a conventional Clinical Data Manager role.
The job primarily involves source document processing, redaction, image/video/document QC, query management, site follow-up, workflow management, and operational team leadership. Candidates with clinical trial operations or clinical data-processing experience may therefore find the position particularly relevant.
Benefits
According to the job posting, Clario offers:
- Competitive compensation and incentives
- Provident Fund
- Medical insurance
- Employee programs and local events
- Modern office facilities
- Remote work flexibility
Salary
The official job description does not disclose a salary range.
For structured-data purposes, an estimated market range of approximately ₹7,00,000–₹14,00,000 per year may be used as a non-employer estimate for a clinical data processing/lead-level position in India. This figure should not be presented as an official Clario salary and should be adjusted or removed if verified compensation information becomes available.
How to Apply
