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Principal Biostatistician (FSP - Permanent Homebased)

Reading, イギリス Full time R1433803

Reading, イギリス| オランダ王国| スロバキア (スロバキア共和国)| ルーマニア| ハンガリー共和国| デンマーク王国| フィンランド共和国| ドイツ連邦共和国| イギリス| スロベニア| スペイン| スウェーデン王国| エストニア共和国| ポーランド共和国| ベルギー王国| Remote

  • Full Time
  • Level: Entry-level, Mid-level, Senior-level

Build a rewarding career in life sciences consulting and forge your own path. Partner with collaborative teams and leaders across unique projects and geographies, delivering innovative solutions to the most complex healthcare problems along the way. Working at IQVIA means changing outcomes for patients one data set, product offering and innovative solution at a time.

As a Consultant at IQVIA, you'll have the opportunity to grow your career and explore opportunities in brand and integrated research solutions, go-to-market strategy, commercial excellence, real world data, financial investor consulting and more.

応募

Success Profile

IQVIAで活躍しているコンサルタントは? 共通するスキル・マインドセットはこちらです。

  • ACHIEVER
  • COMMUNICATION
  • CRITICAL-THINKER
  • ADAPTABLE
  • STRATEGIC
  • DETAIL-ORIENTED

What you can expect

Professional Development

スキル向上できる環境

Highly Specialized

専門分野に特化した働き方

Growth Potential

ステップアップに向けた明確なキャリアパス

Collaboration

共通の目標に向かって、協力し合うチーム

Innovative Projects

複雑な課題を革新的な方法で解決

Best-in-Class Training

知識とスキルを向上するためのトレーニング

大学卒業後、IQVIAに入社し、4年間で素晴らしい経験を積めました。自身のマネージャーはプロフェッショナルとパーソナルな面で成長を促してくれました

Arthur

コンサルタント

Principal Biostatistician (FSP - Permanent Homebased)

Reading, イギリス| オランダ王国| スロバキア (スロバキア共和国)| ルーマニア| ハンガリー共和国| デンマーク王国| フィンランド共和国| ドイツ連邦共和国| イギリス| スロベニア| スペイン| スウェーデン王国| エストニア共和国| ポーランド共和国| ベルギー王国| Remote R1433803
応募

Job Description

Job Description:

The Principal Statistician will be responsible for developing and maintaining standard statistical requirements in data analysis tools and templates, ensuring compliance with industry standards and health authority regulations. These requirements will be aligned with therapeutic area needs and study design considerations.

Key Responsibilities:

  • Develop and maintain standard statistical requirements, including text, definitions, and analysis requirements for Protocols and Statistical Analysis Plans.
  • Create standard tables, listings, and graph mock displays with detailed analysis requirements and rules in Data Presentation Specifications.
  • Maintain data analysis standards at a master level to meet scientific or operational requirements, ensuring formal change management control and versioning.
  • Govern changes to standards, maintaining multiple versions to align with clinical trials and drug development programs.
  • Support the clinical data standards team and standards implementation leads to ensure consistent adoption of standards in studies.
  • Expertise in experimental design, modeling, analysis planning, execution, interpretation, and statistical communications support.
  • Produce clear, concise, well-organized, and error-free analysis programs and statistical reporting content.
  • Establish and maintain effective relationships with internal and external customers.

Educational and Experience Requirements:

  • Master’s or PhD Degree in Statistics.
  • Expertise in SAS or R programming.
  • Working knowledge of relevant regulatory requirements (e.g., GCP, ICH) and industry standards (e.g., ADaM).
  • Relevant operational experience in analysis standards is preferred.
  • Experience in multiple therapeutic areas (e.g., Oncology, Cardiovascular, Immunology, Medical Devices, Neuroscience) is preferred.
  • Ability to work independently with minimal oversight.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

応募

Learn About How We Work

Learn About How We Work

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