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Senior Biostatistician - Global BIOS; Homebased

Remote / Online - Candidates ideally in
Bloemfontein, 9300, South Africa
Listing for: IQVIA
Full Time, Remote/Work from Home position
Listed on 2026-05-18
Job specializations:
  • IT/Tech
    Data Security, Data Analyst, Data Science Manager
  • Research/Development
Job Description & How to Apply Below
Position: Senior Biostatistician - Global BIOS  (Permanent Homebased)

Join us on our exciting journey!

The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability.

IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.

We have one of the largest Biostatistics departments within the industry of around 1,100+ staff, to which we engage the full range of industry‑leading resources and expertise spanning all study phases and therapeutic areas.

Job Overview

As a Senior Biostatistician, you will be given access to cutting‑edge, in‑house technology and opportunities to work on global projects across a variety of therapeutic areas.

You will provide statistical consulting and technical support as it relates to the design, statistical analysis, and regulatory submissions of clinical trial studies.

Acting as a statistical team lead for single, complex studies or groups of studies, you will manage the scope of work and budget, providing revenue and resource forecasts, coupled with preparing proposal text and attending bid defense meetings.

You will also collaborate with medical and programming staff to produce interim reports and final reports, allowing a comprehensive understanding and interpretation of the clinical trial data and outcome.

Requirements
  • BSc or MSc degree in Biostatistics or related field and between 4‑6 years’ relevant experience
  • Familiarity with moderately complex statistical methods that apply to applicable clinical trials
  • Good working knowledge of SAS and CDISC SDTM and ADaM
  • Ability to effectively manage multiple tasks and projects, ability to communicate and explain statistics
Benefits
  • Global exposure
  • Variety of therapeutic areas
  • Collaborative and supportive team environment
  • Access to cutting‑edge and innovative, in‑house technology
  • Excellent career development and progression opportunities
  • Work‑Life Balance with a strong focus on a positive well‑being
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Position Requirements
10+ Years work experience
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