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Technical Officer - Biostatistics & Programming

Lambda Research accelerated
1-4+ years
₹4.0 – ₹8.0 LPA
Ahmedabad, India
15 July 20, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

Technical Officer – Biostatistics & Programming | Lambda Therapeutic Research Ltd.

Job Details

  • Job Title: Technical Officer – Biostatistics & Programming

  • Job Role: Biostatistician (Late Phase Clinical Trials)

  • Company: Lambda Therapeutic Research Ltd.

  • Job ID (Req ID): 1558

  • Location: Ahmedabad, Gujarat, India

  • Department: Biostatistics & Programming

  • Reporting To: Lead – Biostatistics & Programming

  • Job Type: Full-time

  • CTC Range: ₹4.0 – ₹8.0 LPA

  • Posted Date: 20 July 2026


About the Company

Lambda Therapeutic Research Ltd. is a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With over 20 years of experience and 1,500+ employees across India, Poland, the UK, and the USA, the company provides end-to-end clinical research solutions to pharmaceutical, biotechnology, and generic drug companies worldwide.


Job Purpose

The Technical Officer – Biostatistics & Programming will work as a Study Biostatistician for late-phase clinical trials, responsible for statistical study design, sample size estimation, randomization, statistical programming, regulatory support, and clinical study reporting.


Key Responsibilities

  • Act as the Study Biostatistician for late-phase clinical trials.

  • Perform sample size estimation and provide statistical inputs for protocol development and study feasibility.

  • Generate randomization schedules and support IWRS (Interactive Web Response System) activities.

  • Program or review statistical outputs, including Tables, Listings, and Figures (TLFs).

  • Draft and review the Statistical Analysis Plan (SAP).

  • Provide statistical inputs for the Clinical Study Report (CSR).

  • Respond to regulatory authority queries related to statistical activities.

  • Ensure compliance with regulatory guidelines, GCP, and company SOPs.

  • Collaborate with clinical operations, data management, medical writing, and programming teams.


Required Qualifications

  • M.Sc. in Statistics.

  • SAS Advanced or SAS Viya Certification.

  • Experience as a Biostatistician in late-phase clinical trials.

  • Strong knowledge of statistical methods used in clinical research.


Experience Required

  • Minimum 1–3 years of experience as a Biostatistician in late-phase clinical trials within a CRO, pharmaceutical, or biotechnology company.


Preferred Skills

  • Clinical trial biostatistics.

  • Sample size estimation.

  • Statistical Analysis Plan (SAP) preparation.

  • Clinical Study Report (CSR) support.

  • SAS Programming (Base, Advanced, SAS Viya).

  • Tables, Listings, and Figures (TLFs).

  • Randomization schedule generation.

  • IWRS support.

  • Regulatory submissions and statistical query management.

  • Statistical analysis and clinical data interpretation.


One-Line Experience

Candidates with 1–3+ years of experience as a Biostatistician in late-phase clinical trials, along with SAS programming and statistical analysis expertise, are preferred.


Salary Package

  • Official CTC: ₹4.0 – ₹8.0 LPA

  • Market Standard: ₹5.0 – ₹9.0 LPA (depending on SAS expertise, clinical trial experience, and regulatory knowledge).


Why Join Lambda Therapeutic Research?

  • Work with a globally recognized Clinical Research Organization (CRO).

  • Gain exposure to global late-phase clinical trials and regulatory projects.

  • Opportunity to work on statistical design, SAS programming, SAP preparation, and CSR development.

  • Collaborative work environment with experienced biostatistics professionals.

  • Excellent career growth opportunities in biostatistics and clinical data science.