Job Title: Technical Officer – Clinical Data Coordinator
Company: Lambda Therapeutic Research Ltd.
Location: Ahmedabad, India
Req ID: 1540
Date Posted: Feb 10, 2026
Salary (CTC): ₹3,00,000 – ₹6,00,000 per year
Category: Clinical Data Management
Job Overview
The Technical Officer – Clinical Data Coordinator will support clinical data management activities for clinical trials. The role involves eCRF development, data validation, query management, and clinical data documentation to ensure high-quality and compliant clinical trial data. The candidate will also assist with medical coding, reconciliation activities, and training related to clinical data systems.
Key Responsibilities
Develop and test electronic Case Report Forms (eCRF) for clinical studies.
Perform data validation and query management to ensure data accuracy and completeness.
Prepare and maintain Clinical Data Management (CDM) documentation, including:
Data Management Plan (DMP)
Data Validation Plan (DVP)
eCRF Completion Guidelines (eCCG)
Conduct data reconciliation activities between different clinical data sources.
Provide training to study teams on data entry processes and clinical data systems.
Perform medical coding using standard coding dictionaries (e.g., MedDRA, WHO-DD).
Ensure compliance with study protocols, SOPs, and regulatory requirements related to clinical data management.
Support clinical data review and contribute to maintaining high-quality clinical datasets for analysis and reporting.
Required Skills & Competencies
Knowledge of clinical data management processes and systems.
Experience with Electronic Data Capture (EDC) systems.
Familiarity with clinical trial tools such as:
IWRS (Interactive Web Response System)
ePRO (Electronic Patient-Reported Outcomes)
Understanding of data validation, query management, and reconciliation processes.
Basic knowledge of medical coding standards (MedDRA, WHO-DD).
Strong documentation, analytical, and organizational skills.
Good communication and training skills for interacting with study teams.
Experience
Experience working at the site level as a Clinical Research Coordinator (CRC) for late-phase clinical trials.
Practical experience with EDC systems and clinical data management activities is required.
Educational Qualification
M.Pharm (Pharmacology / Quality Assurance)
BDS / BAMS / BHMS
M.Sc. in Life Sciences
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