Senior Statistical Programmer (gn)

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At MorphoSys, our ambition is to redefine how cancer is treated. As a global, commercial-stage biopharmaceutical company, we are driven by the urgency to discover, develop, and deliver groundbreaking medicines, aspiring to give more life for people with cancer.
Our success is created by our people and we bring together exceptional talent from around the world. We are an equal opportunity employer and take pride in offering our colleagues an open, flexible, and diverse work environment. We are looking for people who share our values and are motivated to improve the lives of people impacted by cancer.
Our headquarters are in Planegg, Germany and our U.S. operations are anchored in Boston, Massachusetts. To learn more, visit us at, and follow us on Twitter and LinkedIn.

Your Responsibilities:

  • Oversight and QC of CRO activities in:
    • SDTM and ADAM Datasets development
    • Table / Listing / Figure (TLF) development and validation based on the Statistical Analysis Plan
    • TLF Mock shells development
  • Working with data management in providing programming support for DM activities including data review
  • Performing ad-hoc programming activities utilizing raw data based on internal and external requests
  • Contributing in process development, reviewing and development of SOPs related to statistical programming activities
  • Participate in Clinical Trial Teams, Data Review Teams, etc., and provide inputs from statistical programming perspective
  • Communicating with and/or responding to internal cross-functional teams and clients for project specifications, status, issues or inquiries
  • Collaboration with Statisticians and Data Management in planning study activities and ensuring study timelines are met
  • Performing lead duties when called upon

Job Qualifications:

  • Ideally three or more years of experience in a Pharmaceutical company or a CRO as a SAS Programmer (gn)
  • Bachelor´s or Master´s degree in Informatics, Mathematics, Medical Documentation or other relevant qualification
  • Excellent ability in SAS data manipulation, analysis and reporting skills
  • Extensive experience in implementing CDISC SDTM, CDISC ADaM, and Define standards
  • Good knowledge of Table / Listing / Figure (TLF) programming, including SAS / STAT and SAS macro language and SAS graphic features
  • Good understanding of descriptive and inferential statistics
  • Proficient in industry standards, medical terminology and clinical trial methodologies
  • Submissions experience utilizing define.xml and other submission documents is a plus
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
  • Good communication skills and a good command of English language
  • Ability to work under pressure, flexibility and adaptability

We offer:

  • Creative working in X-functional teams
  • Open and appreciative corporate culture
  • Multicultural environment
  • Working in an attractive, high-quality equipped building with restaurant
  • Free sports and language courses
  • Simplified application for people from Ukraine (fast track via LinkedIn Profile); additional relocation package

Thank you for your interest! We are looking forward to receiving your pertinent application documents. For your application please use exclusively our career portal. We offer not only excellent career prospects, but also support you from the very beginning – even helping you move if necessary.

MorphoSys AG, Semmelweisstraße 7, 82152 Planegg