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Statistical Scientist Job – IQVIA Hiring Now!

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IQVIA

Bachelor, Masters, Ph.D in Biostatistics

7 - 15 LPA

Bangalore

1 - 5 Years

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IQVIA is a global leader in providing advanced analytics, technology solutions, and clinical research services to the life sciences and healthcare industries. With a mission to accelerate medical innovation and improve patient outcomes, IQVIA delivers intelligent insights that help pharmaceutical, biotech, and healthcare organizations make data-driven decisions.

🔗 Learn more about IQVIA: https://jobs.iqvia.com


Job Description

Key Responsibilities:

✔ Statistical Analysis & Protocol Development – Develop statistical methods for study protocols, review case report forms (CRFs), and prepare analysis plans.
✔ Data Management & Quality Control – Ensure high-quality deliverables, validate datasets, and resolve data issues.
✔ Statistical Programming – Write specifications for analysis files, tables, and figures using SAS and other statistical tools.
✔ Client & Team Collaboration – Communicate with clients and study teams on statistical issues, timelines, and results interpretation.
✔ Regulatory Compliance – Ensure adherence to GCP, ICH guidelines, and CDISC standards.
✔ Leadership & Mentorship – Guide junior staff, manage project budgets, and optimize resource allocation.

Essential Functions:

  • Lead statistical aspects of clinical trials, ensuring timely and accurate deliverables.
  • Author Statistical Analysis Plans (SAPs) and review clinical study reports (CSR).
  • Program and validate datasets, tables, listings, and figures (TLFs).
  • Manage database lock and unblinding processes.
  • Contribute to proposals, budgets, and bid defense meetings.

Qualifications & Skills Required

Education & Experience:

  • Bachelor’s degree in Biostatistics (or related field) + 3-5 years of experience OR
  • Master’s degree in Biostatistics + 3-5 years of experience OR
  • Ph.D. in Biostatistics + 1 year of experience

Technical Skills:

✔ Advanced SAS programming (mandatory)
✔ Knowledge of nQuery, R, or other statistical software
✔ Familiarity with CDISC standards (SDTM, ADaM)
✔ Understanding of clinical trial regulations (GCP, ICH guidelines)

Soft Skills:

✔ Strong communication & technical writing skills
✔ Excellent attention to detail
✔ Ability to lead teams & solve complex problems
✔ Time management & multitasking abilities


How to Apply

If you meet the qualifications and are excited about this opportunity, apply before July 4, 2025!

Application Link