Clinical Statistical Programmer

Permanent contract

Avenue Jules Bordet 168 1140 Bruxelles


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Reference number



Operations — Engineering/production

Business industry

Life sciences

Minimum level of experience required

1 to 3 years



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Job description

AKKODIS is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation.

As a Clinical Statistical Programmer, you provide statistical programming expertise to deliver high-quality programs and outputs for analysis of clinical data. It is your responsibility to provide high-quality analysis results on time to support efficient decision making.

What are your responsibilities ?

 Develop Analysis Data Model (ADaM) datasets
 Develop Tables, Figures and Listings / Output and Programming Specification (TFL/OPS) from the Statistical Analysis Plan (SAP) or a related document
 Develop Define.xml and Analysis Data Reviewer’s Guide (ADRG) for data submission
 Program and validate standard ADaM and utility Statistical Analysis Software (SAS) macros or R function/package following good programming practices
 Act as a statistical programming representative within cross-functional study teams and project subteams and provide statistical support and solutions
 Provide input to internal process improvements and/or new statistical programming capabilities
 Maintain current scientific and regulatory knowledge. 



What skills do you bring to the table ?

Bsc. in Statistics, Mathematics, Informatics or equivalent
 At least 2 years of experience as a statistical programmer in the pharmaceutical industry
 Proficient in English (oral and written)
 Good programming skills in SAS (Macro, Structured Query Language (SQL)) and R (function,
 Able to develop, validate and maintain programs
 Basic knowledge of statistical concept and statistics applied to non-clinical, pre-clinical and clinical data
 Basic knowledge of Good Clinical Practice (GCP) and International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines
 Good communication skills, able to build good relationships with internal and external stakeholders  Team player, able to work in a multidisciplinary team
 Able to manage, drive and meet delivery timelines

 Technical knowledge of Clinical Data Interchange Standards Consortium (CDISC) standards (ADaM, Study Data Tabulation Model (SDTM))

What’s the offer you can’t refuse?

As an Akkodis Team Member, you will be:

• Onboarded in your position via a buddy process

• Supported in your career by your Business Manager

• Actor of your training plan and your personal and professional development

• Benefiting from a permanent contract

• Benefiting from a competitive salary package including several extra-legal benefits

Do you any questions? You can contact me at

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