Technical Officer – Clinical Data Management (Early Phase / eCRF Programming)
Company: Lambda Therapeutic Research Ltd.
Location: Ahmedabad, India
Req ID: 1589
Date: May 11, 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, offering end-to-end clinical trial services across early phase, bioequivalence (BABE), pharmacokinetic (PK), and late-phase studies. The company operates across multiple international locations supporting global pharmaceutical and biotech clients.
Role Summary
The Technical Officer – Clinical Data Management (Early Phase) is responsible for:
Designing and developing electronic Case Report Forms (eCRFs / eSource CRFs)
Supporting early-phase clinical trials (BABE / PK studies)
Developing and testing edit checks and data validation rules
Ensuring accuracy and quality of clinical trial data collection systems
Key Responsibilities
1. eCRF / eSource Development
Create electronic Case Report Forms (eCRFs) for in-house studies
Design eSource CRFs for BABE (Bioavailability/Bioequivalence) and PK studies
Ensure CRF design aligns with study protocol requirements
2. Data Validation & Edit Checks
Develop and implement edit checks for clinical data
Test data validation rules for accuracy and completeness
Ensure error-free data capture in clinical databases
3. Testing & Quality Assurance
Perform system testing for CRFs and data entry workflows
Ensure proper functioning of eCRF systems before study use
Support issue resolution during testing phases
4. Early Phase Clinical Study Support
Support early-phase clinical trials (PK/Bioequivalence studies)
Ensure accurate and efficient data collection processes
Work closely with study teams for protocol alignment
Required Qualifications
B.Pharm
B.Sc.
Required Skills & Competencies
Basic understanding of clinical trial data management
Familiarity with eCRF design concepts (preferred)
Attention to detail in data structure and validation logic
Ability to support testing and documentation activities
Good understanding of early-phase (PK / BA/BE) studies (preferred)
Work Environment
Based in Ahmedabad, India
Early-phase clinical trial operations environment
CRO setting focused on BA/BE and PK studies
Structured workflow with clinical data systems and validation tools
Role Impact
Ensures accurate clinical data collection in early-phase studies
Supports integrity of bioequivalence and PK trial data
Improves efficiency of clinical database design and validation
Contributes to regulatory-quality clinical data systems
Career Path
This role can lead to:
Clinical Data Manager
Clinical Database Programmer
SAS Programmer / Biostatistics support roles
Clinical Operations or Data Standards roles
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Sao paulo | Brazil |Attica :
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Manila |Croatia :
Croatia |Zagreb :
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