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Senior Statistical Programmer - PCS

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Primary Location: Oeiras, Lisbon, Portugal Additonal Locations: Barcelona, Spain,ESP; Belgrade, Serbia,SRB; Bloemfontein, South Africa,ZAF; Bloemfontein, South Africa,ZAF; Bratislava, Slovakia,SVK; Bucharest, Romania,ROU; Dublin, Ireland,IRL; Heraklion, Greece,GRC; Ljubljana – Dunajska, Slovenia,SVN; Llanera, Spain,ESP; Madrid, Spain,ESP; Modena, Italy,ITA; Prague, Czech Republic,CZE; Sarajevo, Bosnia,BIH; Sofia, Bulgaria,BGR; Turku, Finland,FIN; Warsaw, Poland,POL; Zagreb, Croatia,HRV Full time R1439038

Job description

Senior Statistical Programmer

PCS

Home-based, office-based, hybrid options available 

Join us on our exciting journey!

Job Overview:

Perform, plan and co-ordinate the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing summaries and (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks.

Program and plan the integration of databases from multiple studies or sources.

Develop and co-ordinate programming documentation including plans and specifications, as appropriate, for complex studies.

Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department, for complex studies.

Fulfil project responsibilities at the level of statistical team lead for single complex studies or group of studies.

Requirements: 

  • Bachelors or Masters in Computer Science, Mathematics or equivalent
  • 5+ years Statistical Programming experience within the Life-Science industry 
  • Experience in SAS® Base, and good knowledge of SAS® graph and SAS® Macros
  • Excellent knowledge of CDISC standards (SDTM and ADaM)
  • Excellent application development skills
  • Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results.
  • Experience as technical team lead, directly engaging clients and coordinating tasks within a programming team
  • In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good Clinical Practice
  • (GCP) and International Conference on Harmonization (ICH) guidelines

Join IQVIA to see where your skills can take you

  • Global exposure 
  • Variety of therapeutic areas
  • Collaborative and supportive team environment 
  • Access to cutting-edge and innovative, in-house technology
  • Excellent career development and progression opportunities 
  • Work-Life Balance, with a strong focus on a positive well-being

#LI-Remote

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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