Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Principal Biostatistican

Fortrea
8+ years
INR 25 LPA – 40 LPA
Bangalore, Pune, India
1 June 17, 2026
Job Description
Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, CPT

Principal Biostatistician

Location: Bangalore / Pune
Work Model: Hybrid
Employment Type: Full Time


Summary of Responsibilities

  • Lead complex studies such as NDA submissions and multi-protocol clinical programs, providing statistical oversight and coordinating activities across multiple locations.

  • Perform project management activities including resource planning, timeline management, and milestone tracking.

  • Serve as DMC Support Statistician by developing DMC Charters and attending DMC meetings under the guidance of Statistical Consultants.

  • Lead the development of complex Statistical Analysis Plans (SAPs) and perform senior reviews of SAPs prepared by other statisticians.

  • Conduct complex statistical analyses and quality review analyses performed by other statisticians.

  • Perform overall statistical review of Tables, Listings, and Figures (TLFs) for complex studies before client delivery.

  • Review CRFs and other study-specific specifications and plans.

  • Perform complex sample size calculations under the supervision of senior statistical staff.

  • Develop statistical sections of study protocols for complex studies under the guidance of Statistical Consultants.

  • Provide statistical input and review for Clinical Study Reports (CSRs).

  • Prepare and review randomization specifications and generate randomization schedules.

  • Mentor and train junior team members while reviewing their work to ensure quality and compliance with departmental procedures.

  • Present technical knowledge during internal seminars, team meetings, and external scientific conferences.

  • Participate in bid defense meetings for complex studies and multi-protocol programs to support business development activities.

  • Act as a Subject Matter Expert (SME) by contributing to procedural documents, process improvements, and strategic initiatives.

  • Represent the department during audits and inspections.

  • Perform additional duties as assigned.


Qualifications (Minimum Required)

  • Master’s degree in a relevant discipline.

  • Equivalent experience may be considered in lieu of educational qualifications.


Experience (Minimum Required)

  • Minimum 8 years of experience in Biostatistics, Clinical Research, or a related field.

  • Strong proficiency in SAS programming and statistical software used for clinical trial analyses.

  • Experience with statistical methodologies including:

    • Non-parametric analysis

    • Linear and non-linear models

    • Categorical data analysis

    • Survival analysis

  • Proven ability to communicate statistical concepts effectively to diverse audiences.

  • Strong understanding of the clinical trial process and its application within clinical development.

  • Experience in:

    • Statistical Analysis Plan (SAP) development

    • Clinical trial analysis and reporting

    • Statistical review and quality control activities

    • Regulatory submission support


Preferred Qualifications

  • Master’s degree or higher in Biostatistics, Statistics, Mathematics, or a related quantitative field.

  • Experience supporting NDA submissions and regulatory interactions.

  • Prior experience leading complex or global clinical development programs.