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Technical Officer - Clinical Data Management

0-3 years
3,00,000 – 6,00,000 per annum
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 | Ahmedabad, India

Req ID: 1304
Posted On: 15 November 2025
Experience Required: Up to 3 years
Salary (CTC Range): INR 3,00,000 – 6,00,000 per annum
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.


About Lambda Therapeutic Research

Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. The organization supports international pharmaceutical, biotech, and generic drug companies through comprehensive end-to-end clinical research services.
With operational hubs in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland), Lambda delivers high-quality clinical trial solutions across multiple therapeutic areas and development phases. The company is recognized for scientific rigor, operational excellence, and global compliance capabilities.


Role Overview: Technical Officer – Clinical Data Management

The Technical Officer, Clinical Data Management, will support late-phase clinical research projects by developing eCRFs, managing data validation processes, coordinating with cross-functional teams, and ensuring adherence to CDM quality standards.
This role is suitable for candidates looking to build depth in data management operations, programming, query handling, and documentation within a global CRO environment.


Key Responsibilities

  • Develop and configure eCRFs for late-phase clinical studies, ensuring accuracy and protocol compliance.

  • Prepare CDM documentation, including Data Management Plan (DMP), Data Validation Plan (DVP), Edit Check Specifications (eCCG), and related study documents.

  • Program and validate edit checks according to study-specific data validation requirements.

  • Perform medical coding activities using standardized dictionaries.

  • Manage and resolve data queries within project timelines.

  • Communicate CDM updates to internal teams and collaborate closely with eDC developers for technical implementation.

  • Support overall CDM deliverables in compliance with project SOPs, timelines, and quality expectations.


Experience Required

  • Up to 3 years of relevant experience in Clinical Data Management within a CRO, pharmaceutical, or life sciences organization.

  • Exposure to eCRF development, edit check programming, query management, CDM documentation, and coding workflows is preferred.


Educational Qualifications

  • M.Pharm (Pharmacology)

  • M.Sc (Life Sciences)