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Job Posting Title Statistician / Statistical Programmer (m/w/d)

IQVIA Holdings Inc.

Munich, Germany

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions and contract research services to the life sciences industry. Formed through the merger of IMS Health and Quintiles, IQVIA applies human data science — leveraging the analytic rigor and clarity of data science to the ever-expanding scope of human science — to enable companies to reimagine and develop new approaches to clinical development and commercialization, speed innovation and accelerate improvements in healthcare outcomes. Powered by the IQVIA CORE™, IQVIA delivers unique and actionable insights at the intersection of large-scale analytics, transformative technology and extensive domain expertise, as well as execution capabilities. With approximately 67,000 employees, IQVIA conducts operations in more than 100 countries.

Our Real-World Evidence (RWE) / Health Economics and Outcomes Research (HEOR) team supports clients from the pharmaceutical and health care industry throughout the entire product life cycle in the optimal positioning of new drugs and medical devices. With tailor-made solutions, our customer focus is on the European Market Access Area (HTA assessments), Health Economic Modelling and Epidemiology.

We are looking for a Statistician who is familiar with the evaluation of clinical studies or would like to become familiar with it. We mainly work in the areas of non-interventional studies (NIS) and HTA (AMNOG) evaluations. Due to our close cooperation with German authorities, the German language is necessary, as well as the willingness to familiarize oneself with regulatory requirements of the IQWiG methods paper, the rules of procedure of the joint Federal Committee (Gemeinsamer Bundesausschuss) and the national/international regulatory authorities.

Your future area of responsibility includes:

  • Planning and analysis of non-interventional studies (NIS)

  • Preparation of the statistical part of the study reports

  • Contribution to the preparation of benefit dossiers (AMNOG) as well as cost-benefit assessments

  • Conducting meta-analyses and indirect comparisons using SAS, R and/or WinBUGS

  • Contact person for customers regarding biometric questions, as well as internal contact person for the project team

  • Programming and validation of analysis data sets, raw data listings and figures with SAS

  • Development of SAS Macros

  • Interdisciplinary cooperation in teams and with our customers

You meet the following requirements:

  • Diploma/Master’s degree in Statistics or in Mathematics with specialization in statistics or a Degree in Medical Documentation or comparable qualification (Bachelor graduates welcome)

  • Knowledge of clinical trials and observational studies

  • Knowledge of SAS and/or R programmingKnowledge of CDISC standards is advantageous

  • A very good command in German and English is mandatory (written & spoken)

  • Interest in the development of new methods

  • Ability to work in a team and communicate well

  • Ideally previous professional experience in the pharmaceutical industry or CROs (Contract Research Organizations), but we would also be happy to give career starters a chance

We can offer you:

  • A competent and growing team

  • On-the-job training and independent work

  • Varied tasks

  • Flexible working hours

  • A flat hierarchy

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At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

Job posted: 2021-03-21

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