Senior Statistical Programmer - Real World Evidence w/m/d (homebased in Germany)
Frankfurt am Main, Germany
vor 6 Tg.

IQVIA’s Real World Evidence Solutions (RWS) group is recruiting Senior Statistical Programmers to join our dynamic team in Europe & Africa

Purpose of Role :

The RWS Senior Statistical Programmer jobs provide statistical SAS programming leadership, expertise and consulting to meet internal and external client needs.

This includes planning and co-ordination of integrated SAS solutions serving the full spectrum of statistical programming for often complex projects

Why you’ll love working with us :

  • Our careers have a greater purpose - alongside a group of diverse, talented colleagues we work daily on making a real positive impact on human lives and overcoming some of the biggest challenges facing global public health
  • We offer opportunities to work with leading international healthcare organizations and the latest healthcare trends
  • You can progress and shape your long-term career in the direction you choose. With access to industry-leading data and experts, you'll find endless opportunities for growth
  • We offer a competitive salary along with other employee focused benefits for health and recreation with flexible hours
  • Please only apply if you match the candidate criteria below.

    Your daily missions would include :

  • The Senior SAS Programmer will perform, plan, co-ordinate and implement SAS programming, testing, and documentation of statistical programs, creating statistical tables, figures and listings, programming of analysis datasets and transfer files and programming quality control checks
  • Interpret project level requirements and develop programming specifications for complex studies
  • Provide advanced technical expertise and independently bring project solutions to the Statistical Programming department
  • Fulfil project responsibilities as technical team lead for single or group studies
  • Directly communicate with internal and client statisticians and clinical team members to ensure understanding of requirements and timelines
  • Estimate programming scope of work, manage resource assignments, communicate project status and negotiate / re-negotiate project timelines
  • Use and promote the use of established standards, SOPs and best practices
  • Provide training and mentoring to SP team members
  • Our perfect candidate needs the following :

  • Statistical programming in SAS within the CRO / Pharmaceutical / Biotechnology / Healthcare industries
  • Advanced knowledge of Base SAS, SAS / STAT, SAS Graph and SAS Macro Language
  • Strong knowledge of SDTM structures and ADaM standards
  • Leadership experience as technical team lead and project lead
  • Masters Degree in computer science or related field and 3 years relevant experience; Bachelor's degree or educational equivalent in computer science or related field and 5 years relevant experience;
  • or equivalent combination of education, training and experience

  • In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Good leadership, organizational, interpersonal and communication skills
  • Ability to independently manage multiple tasks, projects and delegate work to other team members
  • Excellent accuracy, attention to detail and problem-solving skills
  • Able to recognise when negotiating skills are needed
  • Ability to establish and maintain effective working relationships with co-workers, managers and clients
  • Already possess the right to work in the recruiting country without the need for a visa / sponsorship
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