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Technical Officer - Biostatistics & Programming

Lambda Therapeutic Research
Lambda Therapeutic Research
2 years
400000 - 800000
Ahmedabad, India
10 April 22, 2026
Job Description
Job Type: Full Time Education: M.Sc. (Statistics) + SAS (Advance / Viya certifications) 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

 


Organisational Overview

Company Name: Lambda Therapeutic Research Limited

Lambda Therapeutic Research Limited is a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with international operations in:

  • Mehsana (India)
  • Warsaw (Poland)
  • London (UK)
  • Pittsburgh (USA)
  • Las Vegas (USA)
  • Fargo (USA)

The organization has a workforce of 1500+ employees globally.

Core Expertise

Lambda provides full-spectrum clinical trial solutions backed by:

  • Over 20 years of industry experience
  • Expertise in biopharmaceutical and generic sectors
  • Advanced technologies and therapeutic knowledge

Key Strengths

  • Strong leadership with experienced industry professionals
  • Commitment to quality, safety, and efficiency
  • Focus on timely and effective product development

Work Culture

Lambda emphasizes:

  • Hiring skilled and motivated professionals
  • Encouraging excellence and innovation
  • Recognizing employees as the foundation of quality delivery

Job Details

  • Job Role: Biostatistician (Late Phase Clinical Trials)
  • Reporting To: Lead – Biostatistics & Programming
  • Department: Biostatistics & Programming
  • Location: Ahmedabad

Overall Purpose of the Role

  • Act as a Study Statistician for late-phase clinical trials
  • Contribute to study design, execution, and statistical analysis

Key Responsibilities

1. Study Design & Planning

  • Perform sample size estimation
  • Provide protocol inputs
  • Conduct study feasibility assessments for late-phase trials

2. Randomization & Trial Support

  • Generate randomization schedules
  • Provide support for IWRS (Interactive Web Response System)

3. Statistical Analysis & Reporting

  • Program or review:
    • Statistical results
    • Tables
    • Listings
    • Figures (TLFs)

4. Documentation & Reporting

  • Draft Statistical Analysis Plan (SAP)
  • Provide statistical inputs for Clinical Study Report (CSR)

5. Regulatory Support

  • Respond to regulatory queries related to statistical activities