Technical Officer – Clinical Data Management (Late Phase – CDM LP)
Company: Lambda Therapeutic Research Ltd.
Location: Ahmedabad, India
Req ID: 1588
Date: May 12, 2026
CTC Range: ₹3,50,000 – ₹7,00,000 per annum
Company Overview
Lambda Therapeutic Research Ltd. is a global Clinical Research Organization (CRO) headquartered in India. It provides end-to-end clinical trial services across early and late-phase studies, supporting global pharmaceutical, biotech, and generic drug development programs.
Role Summary
The Technical Officer – Clinical Data Management (Late Phase) is responsible for:
Designing and validating electronic Case Report Forms (eCRFs)
Supporting late-phase clinical trial data management activities
Handling data validation, query management, and medical coding
Supporting study lifecycle activities from start-up to close-out
Key Responsibilities
1. eCRF Design & Development
Design and develop electronic Case Report Forms (eCRFs)
Support testing and validation of CRF structures
Conduct eCRF training sessions for study teams
Ensure CRF alignment with protocol requirements
2. Data Validation & Query Management
Perform data validation checks
Manage and resolve clinical data queries
Ensure accuracy, consistency, and completeness of clinical trial data
3. Medical Coding
Perform medical coding of clinical data
Ensure standardized terminology usage (e.g., MedDRA/WHO-DD concepts)
Support coding review and reconciliation
4. Data Reconciliation
Reconcile external data sources with clinical databases
Ensure consistency across clinical systems
Support resolution of data discrepancies
5. Clinical Study Lifecycle Support
Participate in:
Study start-up
Study conduct
Study close-out
Attend project meetings and contribute updates
Support operational execution across study phases
6. Documentation & Compliance
Maintain CDM documentation and records
Ensure compliance with study protocols and SOPs
Support audit-ready documentation practices
Key Deliverables
eCRF development, testing, and training
Data validation and query management
Medical coding activities
Data reconciliation and CDM documentation
Required Qualifications
M.Pharm
M.Sc. (Life Sciences)
BHMS / BAMS / BDMS
Required Skills & Competencies
Understanding of clinical data management (CDM) processes
Knowledge of eCRF design and validation workflows
Familiarity with query management systems
Basic understanding of medical coding concepts
Attention to detail and data accuracy
Ability to work in cross-functional clinical teams
Work Environment
Based in Ahmedabad, India
Late-phase clinical trial environment
CRO-based data management operations
Exposure to global clinical study workflows
Role Impact
Ensures accuracy and integrity of late-phase clinical trial data
Supports regulatory-quality clinical databases
Enables smooth execution of clinical study lifecycle
Contributes to reliable submission-ready clinical datasets
Career Path
This role can lead to:
Clinical Data Manager
CDM Lead / Project Lead
Clinical Database Programmer
Clinical Operations / Biostatistics support roles
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