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Technical Officer - Biostatistics & Programming

0-2 years
INR 6,00,000 – 8,00,000
10 Oct. 7, 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

Job Title: Technical Officer – Biostatistics & Programming

Req ID: 1326
Date Posted: September 28, 2025
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range: INR 6,00,000 – 8,00,000


Organizational Overview

Lambda Therapeutic Research is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with facilities in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland).

Key Highlights:

  • Provides comprehensive end-to-end clinical research services to global innovator, biotech, and generic pharmaceutical industries


Department: Biostatistics & Programming

Designation: Technical Officer
Education Required: M.Sc. in Biostatistics + SAS Programming certification
Experience Required: Early phase statistical data analysis and reporting experience


Job Overview

The Technical Officer will support early phase clinical trials through statistical analysis, reporting, and regulatory compliance, using specialized statistical software.


Key Responsibilities

  • Perform early phase (BABE) statistical data analysis and reporting

  • Provide statistical input for study protocols and sample size estimations

  • Support regulatory query responses and investigations

  • Work proficiently with Phoenix WinNonlin and SAS software


Required Competencies

  • Strong statistical analysis skills

  • Proficiency in SAS & Phoenix WinNonlin

  • Understanding of early phase clinical trial data

  • Attention to detail and regulatory compliance