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Technical Officer – Clinical Data Management

0-2 years
3-5 LPA
10 Dec. 2, 2025
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc., Lifesciences graduate 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 

Lambda Therapeutic Research Ltd. | Ahmedabad, India

Experience Required: Fresher to 2 Years
CTC Range: ₹3,00,000 – ₹5,00,000 per annum
Job ID: 1439
Posted On: 7 November 2025
Location: Ahmedabad, India


About the Organisation

Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad. With established operations in India (Ahmedabad, Mehsana), USA (Las Vegas), Canada (Toronto), Spain (Barcelona), UK (London), and Poland (Warsaw), Lambda provides end-to-end clinical research solutions to innovator companies, biotech sponsors, and generic pharmaceutical organizations worldwide.
The company is known for scientific excellence, operational quality, and its comprehensive support across early-phase, late-phase, and Bioequivalence/Bioavailability (BA-BE) studies.


Role Overview

The Technical Officer will support core Clinical Data Management (CDM) functions, contributing to data quality, system configuration, coding activities, and trial documentation.
This position is ideal for freshers and early-career professionals seeking to build expertise in CDM and late-phase clinical research operations.


Key Responsibilities

Clinical Data Management

  • Design and update eCRFs based on protocol requirements.

  • Perform data validation and manage data queries end-to-end.

  • Support user trainings and study-level data management tasks.

Late Phase Study Support

  • Participate in planning, execution, monitoring, and close-out activities for late-phase clinical trials.

Medical Coding

  • Apply accurate medical coding to concomitant medication data captured in electronic data capture (eDC) systems.

Documentation & Compliance

  • Prepare and maintain CDM documentation in alignment with organizational processes and regulatory expectations.

  • Ensure timely delivery of all CDM outputs as per study timelines.


Key Deliverables

  • eCRF development and testing

  • Query management and issue resolution

  • Medical coding accuracy

  • CDM documentation and reporting


Experience Required

  • Fresher to 2 years of experience in:

    • Working as a Clinical Research Coordinator (CRC) on eDC platforms

    • Supporting Clinical Data Management environments as a Data Manager or Data Validator

(Your job portal may highlight this role as fresher-friendly.)


Educational Qualification

Candidates with any of the following qualifications are eligible:

  • BDS / BHMS / BAMS

  • M.Pharm

  • M.Sc. in Life Sciences or Clinical Research