Freshers Biostatistician Jobs at Inductive Quotient Analytics (IQA), Apply on Biotecnika
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Freshers Biostatistician Jobs at Inductive Quotient Analytics (IQA), Apply on Biotecnika

Looking to start your career in clinical data science? Freshers Biostatistician Jobs at Inductive Quotient Analytics (IQA), Apply on Biotecnika is now one of the most searched opportunities for life science and bioinformatics graduates in 2025. This role offers hands-on exposure to statistical analysis, clinical datasets, regulatory standards, and SAS programming—making it an ideal entry point for candidates aiming to build a career in biostatistics and clinical research.

Job Title: Biostatistician

Company: Inductive Quotient Analytics (IQA)

Experience: 0–1 Year (Freshers Eligible)

Location: Hyderabad (Local candidates preferred)

Salary Range: ₹2.4–3 LPA

Requirement: Immediate Joiners

About Inductive Quotient Analytics

Inductive Quotient Analytics (IQA) was founded by seasoned statisticians and technology
leaders with over two decades of industry expertise. We specialize in advanced digitization
solutions, AI/ML-powered analytics, and comprehensive data science services for the Life
Sciences sector. Our mission is to enable smarter decision-making, accelerate innovation, and enhance healthcare outcomes through robust, data-driven solutions.

Role Overview

We are looking for a motivated and detail-oriented Biostatistician to support statistical
activities across clinical studies. This role is ideal for individuals passionate about clinical
data analysis and looking to build a strong foundation in biostatistics within a regulated
environment.

Roles & Responsibilities

• Perform biostatistical analyses in accordance with organizational quality standards,
SOPs, ICH-GCP, and applicable regulatory guidelines.
• Analyze clinical trial datasets and generate accurate statistical outputs.
• Validate statistical results to ensure accuracy, consistency, and reproducibility.
• Assist in developing and updating statistical SOPs, templates, and standard
methodologies.
• Support communication and interactions with regulatory agencies, as required.

Preferred Technical & Professional Expertise

• Understanding of ICH-GCP (E6) and ICH-E9 guidelines.
Basic knowledge of BASE SAS and SAS programming.
• Familiarity with CDISC standards, including SDTM and ADaM.
• Awareness of regulatory norms governing clinical data and statistical reporting.

Good to Have

• Strong communication, interpersonal, and teamwork skills.
• Good analytical thinking with a clear grasp of coding logic and algorithms.
• Creative mindset with the ability to think independently and innovatively.

Qualifications

• Bachelor’s or Master’s degree in Life Sciences, Pharmacology, Bioinformatics,
Biostatistics, or related disciplines.

CLICK HERE TO APPLY ONLINE

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