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)
Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | Tarasadi | Vadodara | Vapi |Maharashtra :
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