Technical Statistical Programmer

☞ Argenx

見る: 160

更新日: 16-11-2025

場所: Ghent East Flanders

カテゴリー: IT-ソフトウェア IT-ハードウェア/ネットワーキング 情報技術

業界:

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仕事内容

We are currently looking for a Statistical Programmer who will support the programming and biostatistics team for diverse programming tasks, supporting the clinical development programs within argenx. The tasks mainly focus on the creation and validation of standardized programs and macros that support creation of TLF’s or analysis datasets. Also support the development and maintenance of a data repository with corresponding standardized reporting tools. Work on automation of repetitive programming tasks and manage and maintain the SAS computing environment. Support other programmers with technical expertise and support other functional areas within the company by delivering high quality data in a timely manner.

Key Accountabilities/Responsibilities:

  • Develop, review, document and perform validation of SAS programs and macros.

  • Support the development of data repositories, pooling multiple studies

  • Create standard reports in different output formats

  • Automate programming tasks within the SAS environment

  • Generate programmed QC checks

  • Build utilities in support of other programming tasks

  • Design new tools or review existing tools and improve where needed.

  • Develop, validate and document programs for ad-hoc analyses.

  • Assess the time needed to develop programs and can at least partially self-manage the work.

  • Take responsibility to deliver a support in time in function of stakeholders needs.

.Desired Skills and Experience:

  • Excellent knowledge of SAS is a must. Knowledge of other programming languages like R, Java is a plus.

  • Passionate about programming. Always looking for better solutions, but has a critical view for not overengineering software.

  • Is able to demonstrate leadership in development of general purpose tools.

  • Is creative, brings ideas to the table and can perform well when given creative freedom.

  • Display good communication skills, is able to explain ideas and can also listen well to ideas from others, can be self-critical.

  • Thorough knowledge of and experience with CDISC standards is desired.

  • Knowledge of ICH-GCP and other applicable legislation, with good understanding of clinical data and pharmaceutical development.

  • Bachelors or higher degree in Science, Statistics, Information Technology or equivalent combination of education and related work experience.

  • Minimum of 10 years of professional experience desired.

Offer:

  • A competitive salary package with benefits;

  • A work environment in a human-sized, dynamic, rapidly growing biotech company

#LI-DNI

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締切: 31-12-2025

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