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2+ years
₹3,00,000 – ₹5,00,000 per annum
10 Nov. 11, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Technical Officer – Clinical Data Management

Company: Lambda Therapeutic Research Ltd.
Req ID: 1439
Location: Ahmedabad, India
Date Posted: 07 Nov 2025
CTC Range: ₹3,00,000 – ₹5,00,000 per annum


Company Overview

Lambda Therapeutic Research is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India.
The organization operates across key global locations including:

  • Mehsana (India)

  • Las Vegas (USA)

  • Toronto (Canada)

  • Barcelona (Spain)

  • London (UK)

  • Warsaw (Poland)

Lambda provides end-to-end clinical research services to innovator, biotech, and generic pharmaceutical companies worldwide.


Job Summary

The Technical Officer will support Clinical Data Management (CDM) activities across late-phase clinical trials, ensuring high-quality data capture, validation, and documentation.


Key Responsibilities

Clinical Data Management

  • eCRF design, development, testing, and updates

  • Data validation and query management

  • Conducting and participating in CDM-related trainings

  • Supporting planning, execution, and close-out phases of late-phase clinical trials

Medical Coding

  • Coding concomitant medication data using standardized medical dictionaries within eDC systems

Documentation

  • Preparation and maintenance of CDM documentation as per study requirements


Key Deliverables

  • High-quality eCRF development and maintenance

  • Effective query management and resolution

  • Accurate medical coding

  • Complete and compliant CDM documentation


Required Experience

  • Up to 2 years’ experience as:

    • Clinical Research Coordinator (CRC) with hands-on work in eDC platforms, or

    • Clinical Data Manager / Data Validator in a CDM department


Education

Candidates should possess one of the following:

  • BDS, BHMS, or BAMS

  • M.Pharm

  • M.Sc. (Life Sciences / Clinical Research)