Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook
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)