Expires soon KEYRUS

STATISTICAL PROGRAMMER

  • V.I.E.
  • Waterloo (Waterloo Regional Municipality)
  • Master, Bac +5

Job description

Entreprise:
Keyrus Biopharma is an international full-service CRO with a reputation for transparency and integrity, highly focused on being able to deliver with excellence. Our ‘human’ approach to service provision is what differentiates us from our competitors. Combined with our high caliber staff, this approach has allowed us to become a key player in clinical research.
From early
- to late-stage clinical development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical Information.
Poste et missions:
The Statistical Programmer position is part of the Statistical Programming Group (within the Biostatistics Department), and is responsible for developing SAS programs for the analysis of clinical data in accordance to departmental SOPs , guidelines and international standards: CDISC SDTM & ADaM.
Main activities
- Represent data analysis function in multi-disciplinary teamwork
- Create, review, or approve programming plans and specifications at project and study level
- Program, according to specifications, analysis datasets, tables, listings, and figures for phase I-IV clinical trials and publications
- Review key study documents produced by other functions (e.g. CRFs, data management plans, SAPs, clinical study reports, etc.)
- Develop or assist in the development of procedures and/or programs to transfer data from legacy data, outside sources, such as CROs or clinical laboratories, to in-house CDISC Compliant structures (SDTM/ADaM)
- Support quality control of deliverables related to biostatistics
- Maintain records for all assigned projects and archiving of trial/project analysis and associated documentation.
- Contribute to the creation and maintenance of department SOPs related to clinical data analysis.
Profil:
- Bachelor’s Degree in Computer Science, Statistics, Mathematics, Life Sciences or other relevant scientific fields Master’s Degree preferred
- Minimum of 1 years of experience in developing programs using the SAS system
- Good Knowledge of statistics and drug development process
- Excellent proficiency in programming with SAS
- Knowledge and/or experience working with CDISC SDTM and ADaM compliant data sets is an asset
- Solid verbal and written communication skills in French and English
- Must be able to work independently on multiple projects concurrently
Come and join us in Belgium !
What are the advantages to work at Keyrus Biopharma Belgium?
- You will boost your career at the international level. You will work with colleagues from all over the world on global projects. You will work with international teams, projects and clients!
- You will enjoy the famous Belgian culture focused on open, simplicity and work-life balance!
- You will have a high quality of life in Belgium (Cost of life lower than other EU big capital cities), famous Belgian gastronomy, lots of green areas…).
- You will work in our offices located in the middle of countryside. You will have the opportunity to attend some internal events, to do sport with colleagues, to possibly work from home if needed and to have flexibility in your working hours.
- Brussels is also a crossroads in Europe. If you like travelling, don’t miss the closest cities like Paris, London or Amsterdam!
- Each new comer is welcomed with a varied integration program. We invest considerable time and resources in training our staff (technical and non-technical courses). You will join a dynamic and international environment with enthusiastic and professional colleagues.
Interest ? Please send your resume and motivation letter in English.

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