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Technical Officer - Biostatistics & Programming

Lambda Therapeutic Research
2-5 years
₹4–8 LPA
Ahmedabad, India
15 July 7, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Analytical Characterization, Dissolution Testing, Experimental Design, GMP/cGMP Compliance, HPLC, HPLC Analysis, Pre-formulation Studies, Regulatory Filing Support, Root Cause Analysis (RCA), Technology Transfer, UPLC

Technical Officer – Biostatistics & Programming

Company: Lambda Therapeutic Research Ltd.
Location: Ahmedabad, India
Department: Biostatistics & Programming
Employment Type: Full-Time

Experience: 2–5 years of experience as a Biostatistician in late-phase clinical trials with hands-on expertise in statistical analysis, SAS programming, and clinical trial reporting.
Salary Package: ₹4–8 LPA (As per company CTC range; final compensation depends on candidate experience, SAS expertise, and clinical trial exposure.)


Role Overview

The Technical Officer – Biostatistics & Programming is responsible for providing statistical support for late-phase clinical trials, including study design, sample size estimation, randomization, statistical programming, analysis, and regulatory documentation. The role collaborates with cross-functional clinical teams to ensure high-quality statistical deliverables that meet regulatory and project requirements.


Key Responsibilities

Biostatistics & Study Design

  • Serve as the study statistician for late-phase clinical trials.

  • Perform sample size estimation based on study objectives and statistical assumptions.

  • Provide statistical inputs during protocol development and study feasibility assessments.

  • Support study design and statistical methodology selection.


Randomization & Statistical Programming

  • Generate randomization schedules for clinical studies.

  • Provide statistical support for Interactive Web Response Systems (IWRS).

  • Develop or review statistical programming outputs using SAS.

  • Generate and validate:

    • Statistical Results

    • Tables

    • Listings

    • Figures (TLFs)

  • Ensure accuracy and quality of statistical deliverables.


Statistical Analysis & Reporting

  • Prepare and review Statistical Analysis Plans (SAPs).

  • Perform statistical analyses according to approved SAPs.

  • Provide statistical inputs for Clinical Study Reports (CSRs).

  • Ensure statistical outputs meet regulatory and sponsor requirements.


Regulatory & Compliance Support

  • Prepare responses to regulatory authority queries related to statistical analyses.

  • Ensure compliance with applicable regulatory guidelines and industry standards.

  • Maintain documentation supporting statistical analyses and programming activities.

  • Collaborate with regulatory and clinical teams during submissions.


Cross-Functional Collaboration

  • Work closely with Clinical Operations, Data Management, Medical Writing, and Regulatory teams.

  • Support project planning and timely completion of statistical deliverables.

  • Participate in process improvement initiatives within the Biostatistics & Programming function.

  • Assist in maintaining high-quality standards across statistical activities.


Educational Qualification

  • M.Sc. in Statistics (Mandatory).

  • SAS Advanced or SAS Viya Certification is preferred.


Required Experience

  • 2–5 years of experience as a Biostatistician in late-phase clinical trials.

  • Hands-on experience in statistical analysis and clinical trial reporting.

  • Experience preparing Statistical Analysis Plans (SAPs) and Clinical Study Reports (CSRs).

  • Experience supporting regulatory submissions and responding to statistical queries.


Technical Skills

  • Strong knowledge of biostatistics and clinical trial methodologies.

  • Advanced proficiency in SAS Programming (Base SAS, Advanced SAS, or SAS Viya).

  • Experience with:

    • Sample size calculation

    • Randomization schedule generation

    • Statistical programming

    • TLF generation (Tables, Listings, Figures)

    • IWRS support

  • Understanding of ICH-GCP guidelines and regulatory requirements.

  • Proficiency in Microsoft Office applications.


Key Competencies

  • Strong analytical and statistical problem-solving skills.

  • Excellent attention to detail and data accuracy.

  • Strong programming and validation skills.

  • Effective written and verbal communication abilities.

  • Good organizational and time management skills.

  • Ability to manage multiple clinical projects simultaneously.

  • Strong collaboration and stakeholder management skills.

  • Commitment to quality, compliance, and timely project delivery.