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Emplois de Programmeur

Les exigences pour les programmeurs sont variées et ce métier est très demandé. Les points principaux de ce travail sont le développement d'applications et de logiciels, où d'une part de nouveaux programmes, de nouvelles utilisations sont inventés, et d'autre part des programmes déjà existants sont améliorés. Le travail dépend des exigences de l'employeur. Pour son travail, le programmeur se spécialise dans des domaines précis, comme PHP, Java, CNC ou SAP. Pour ce poste, on recherche des personnes qui aiment développer des solutions pour le client en groupe et qui sont ensuite capables de lui en expliquer l'utilisation simplement. Les programmeurs peuvent travailler des les entreprises de logiciels, les banques, les assurances et les administrations publiques. En Suisse, les programmeurs peuvent aussi travailler en tant qu'indépendants, ce qui leur permet d'organiser leur travail comme ils le souhaitent et peut aussi leur ouvrir la voie à un poste fixe dans une entreprise.

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Senior Statistical Programmer

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Senior Statistical Programmer


About Idorsia Pharmaceuticals Ltd

Idorsia Ltd is reaching out for more - We have more ideas, we see more opportunities and we want to help more patients.

In order to achieve this, we will develop Idorsia into one of Europes leading biopharmaceutical company, with a strong scientific core.

Headquartered in Switzerland - a European biotech hub - Idorsia is specialized in the discovery and development of small molecules, to transform the horizon of therapeutic options. Idorsia has a broad portfolio of innovative drugs in the pipeline, an experienced team, a fully-functional research center, and a strong balance sheet the ideal constellation to bringing R&D efforts to business success.

Idorsia was listed on the SIX Swiss Exchange (ticker symbol: IDIA) in June 2017 and has over 600 highly qualified specialists dedicated to realizing our ambitious targets.


Job Responsibilities


  • Responsible for the implementation and use of programs to effectively analyze and report clinical trial data as the trial lead programmer
  • Responsible for the review of trial documentation and providing feedback from statistical programming perspective, as well as study set-up in the reporting environment
  • Responsible for the definition of project and trial analysis data sets and metadata
  • In agreement with the lead statistical programmer and/or statistician, designs and implements trial and project analysis data sets and metadata including complex data derivations, data mapping and data pooling
  • Manage critical issues within the project by pro-actively suggesting solutions to the lead statistical programmer and/or statistician
  • Develops programs and generates tables, listings and figures for trial or project specific reports and statistical analyses in agreement with trial documentation and guidelines from the principal statistical programmer and/or the statistician
  • Performs and documents quality control (QC) activities as per Idorsia standard operating procedures (SOPs), working practices, and guidance from the lead statistical programmer


Candidates Requirements


  • University degree (or equivalent) preferably in mathematics, informatics or other scientific discipline
  • Advanced knowledge of programming in SAS and of statistical analyses in clinical trials
  • Min of5yearsexperience in statistical programmingwithin a pharmaceuticalcompany or a clinical research organization (CRO)
  • Experience in the review of Statistical Analysis Plans, study set-up and review of study specificdocuments, e.g. Clinical Protocol, CRF, annotated CRF, data validation guidelines
  • Knowledge of all aspects of clinical trials from initial study set-up to study completion with anexcellent understanding of the roles and responsibilities of all related disciplines, e.g. Biostatisticsand Clinical Data Management
  • Good knowledge and understanding of CDISC, especially SDTM and ADaM
  • Basic knowledge of R, knowledge of other programming languages and of data managementprinciples and tools is an asset
  • Proven record to work independently, analyze problems and formulate ideas in a structured and logicalmanner
  • Knowledge of international clinical research regulations and requirements (ICH-GCP)
  • Excellent interpersonal and communication skills
  • Fluent in English (written and spoken)


What Idorsia offers

  • Exciting opportunities for development and professional growth within our dynamic organization
  • A collaborative and solution oriented enviroment where you can make a difference
  • An innovative and open culture in a truly multicultural environment
  • A competitive salary and generous social benefits


Work Location:Allschwil


Business Area:Global Clinical Development

Schedule:Fulltime, office based

Job Type:Permanent

Job ID:1446


If you are interested, please click on apply now.

Please be informed that if you are selected for this position, your employment will be subject to a pre-employment background screening process, of which you would be informed in greater detail in due course.

Please note Idorsia operates a strictly-controlled list of preferred recruitment partners. For those partners who have no valid, signed Master Service Agreement in place with Idorsia all unsolicited resumes, CVs, anonymous profiles, or any other candidate details submitted through our website or to personal e-mail accounts of employees of Idorsia Pharmaceuticals (including any of its subsidiaries, affiliates or related companies) are considered the property of Idorsia Pharmaceuticals and are not subject to payment of any form of introduction, placement or referral fees.

Allschwil / Basel area - Allschwil

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