Description
My client, pharmaceutical organisation based in Brussels area is currently looking for a SAS clinical Programmer to complete its team.
This mission consists in joining an existing project team working on a filing project in the Bone Therapeutic Area on a statistical programming role.
The team is in charge of clinical study analysis and reporting (from AdAM derivation to creation of Tables, Figures, Listings) across multiple studies as well as in parallel developing and validating filing deliverables (Statistical Review Aids, CRT, integrated analysis, OSI packages).
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Multiple years (preferably 5) of relevant clinical trial SAS experience in analysis and reporting.
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Proficient SAS programming skills with mastery of SAS/STAT SAS/BASE, SAS macro language. SAS/GRAPH is a nice to have. SAS/MACRO is a must for this mission.
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Capacity to interface with clinicians, statisticians and data managers as statistical programmer in charge of a clinical trial.
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Team oriented person.
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Capacity to work independently or under the guidance of a senior programmer.
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Capacity to quickly read SAS code (including MACRO code) developed by others and understand them in the context of clinical trials.
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Knowledge and practice of CDISC SDTM and ADaM data standards. ADaM is a must have for this mission.
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Ability to work complying to the company programming SOPs, project data standards and macro library as well as capacity to develop project specific code independently under company SOPs.
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Strong and proven experience of work with clinical trial data in support of safety and efficacy analysis.
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Able to read, write and speak fluently in English. English writing skills are a must for this mission.
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Experience with SAS on PC and UNIX platforms.
Interested, then please send us your CV ASAP.