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Lead Analyst Bio Statistician, Clinical Research Stryker-New

stryker
6-9 years
18 LPA - 35 LPA
Bangalore, India
1 June 22, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Lead Analyst – Biostatistics (Clinical Research)

Location: Bangalore, India
Company: Stryker
Department: Clinical Affairs / Clinical Research
Employment Type: Full-Time (Hybrid)


Role Summary

The Lead Analyst – Biostatistics is responsible for providing statistical leadership and analytical support for clinical research programs, clinical studies, and regulatory submissions. The role involves designing statistical methodologies, developing Statistical Analysis Plans (SAPs), performing complex statistical analyses, SAS programming, interpreting clinical data, and supporting publication and regulatory activities.

The position works closely with Clinical Affairs, Medical Writing, Regulatory Affairs, Data Management, and Clinical Development teams to ensure scientifically sound and regulatory-compliant clinical research outcomes.


Key Responsibilities

Statistical Planning & Study Design

  • Provide statistical expertise for clinical development programs and clinical studies.

  • Participate in protocol development and study design discussions.

  • Recommend appropriate endpoints, sample size calculations, and analysis methodologies.

  • Contribute to optimization of study designs and clinical research strategies.

Statistical Analysis & Reporting

  • Develop Statistical Analysis Plans (SAPs).

  • Define derived variables and data handling methodologies.

  • Create mock tables, listings, and figures (TLFs).

  • Perform statistical analyses and validation activities.

  • Interpret study results and provide scientific recommendations.

  • Contribute to Clinical Study Reports (CSRs).

SAS Programming

  • Develop and validate SAS programs for:

    • Analysis datasets

    • Tables, Listings & Figures (TLFs)

    • Derived datasets

    • Adverse Event analyses

    • Survival analyses

    • Data cleaning and reconciliation

  • Perform quality control and validation of SAS outputs.

  • Create programming specifications and documentation.

Clinical Trial Data Analysis

  • Analyze data from:

    • Clinical Trials

    • Medical Device Studies

    • Pharmaceutical Studies

    • Biotechnology Research

  • Perform:

    • Regression Analysis

    • Survival Analysis

    • Categorical Data Analysis

    • Non-parametric Analysis

    • Linear & Non-linear Modeling

Regulatory Support

  • Support submissions to:

    • FDA

    • ISO Authorities

    • Global Regulatory Agencies

  • Provide statistical responses to regulatory queries.

  • Ensure compliance with:

    • FDA/CFR Guidelines

    • ISO 14155

    • GCP Requirements

Publications & Scientific Communication

  • Collaborate with:

    • Clinical Scientists

    • Medical Writers

    • Key Opinion Leaders (KOLs)

  • Support preparation of:

    • Manuscripts

    • Posters

    • Abstracts

    • Scientific Publications

  • Present statistical findings to internal and external stakeholders.

Data Management & Systems

  • Work with:

    • Electronic Data Capture (EDC) Systems

    • Electronic Health Records (EHR) Systems

  • Support data quality, validation, and integrity activities.

Leadership & Mentoring

  • Guide and mentor junior statisticians and programmers.

  • Review statistical outputs and programming deliverables.

  • Provide technical training and statistical consultation.


Required Qualifications

Education

  • M.Sc / M.Stat / M.Tech (Biostatistics, Statistics, Mathematics)
    OR

  • PhD (Biostatistics, Statistics, Mathematics, Epidemiology, Related Field)


Experience

  • 6–9 years of Biostatistics experience.

  • Experience in:

    • Clinical Research

    • Pharmaceutical Industry

    • Biotechnology Industry

    • Medical Device Industry