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Technical Officer

Lambda Research Accelerated
Lambda Research accelerated
2 years
300000 - 500000
10 Dec. 29, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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.
Location: Ahmedabad, India
Employment Type: Full-Time
CTC Range: ₹3,00,000 – ₹5,00,000 per annum


About Lambda Therapeutic Research

Lambda Therapeutic Research Ltd. is a globally recognized full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with strategic operations in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland). We provide end-to-end clinical research services to innovator, biotech, and generic pharmaceutical companies worldwide, supporting the development of safe and effective therapies.


Role Overview

We are seeking a Technical Officer to join our Clinical Data Management (CDM) team. The ideal candidate will actively contribute to late-phase clinical trials, managing eCRF design, data validation, query resolution, and medical coding for concomitant medications. This role requires strong attention to detail, regulatory awareness, and experience in electronic data capture (eDC) systems.


Key Responsibilities

  • Design, develop, test, and update electronic Case Report Forms (eCRFs) in alignment with study protocols

  • Perform data validation and query management to ensure accuracy, completeness, and compliance of clinical trial data

  • Conduct medical coding for concomitant medications and adverse event data captured in eDC

  • Maintain CDM documentation in compliance with SOPs and regulatory guidelines

  • Participate in training sessions and support team knowledge sharing for CDM best practices

  • Support planning, execution, and close-out activities for late-phase clinical trials


Required Qualifications

  • Educational Background:

    • BDS / BHMS / BAMS

    • M. Pharma

    • M.Sc. in Life Sciences or Clinical Research

  • Experience:

    • Up to 2 years as a Clinical Research Coordinator (CRC) on eDC platforms

    • Hands-on experience in CDM activities as a Data Manager or Data Validator

  • Strong understanding of clinical trial processes, GCP, and regulatory requirements

  • Excellent analytical, communication, and documentation skills


Why Join Lambda Therapeutic Research

  • Work in a global CRO environment with exposure to international clinical trials

  • Gain hands-on experience in clinical data management, eDC systems, and medical coding

  • Competitive salary and benefits aligned with experience

  • Opportunities for career growth and skill development in clinical research


How to Apply

Interested candidates may submit their updated resume to hr@lambdatherapeutic.com with the subject line:
“Application – Technical Officer (Clinical Data Management)”

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