Senior Statistical Programmer

Senior Statistical Programmer

Job Title: Senior Statistical Programmer
Contract Type: Permanent
Location: Frankfurt am Main, Hessen
Salary: €60000 - €80000 per annum
Reference: LHMUC_1580482301
Contact Name: Jamie Haerewa
Contact Email:
Job Published: January 31, 2020 14:51

Job Description

JOB TITLE Statistical Programmer



CITY Munich

JOB TYPE Full time



Perform, plan, co-ordinate and implement the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in crafting statistical tables, figures, and listing and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal and external clients and (iii) the programming quality control checks for the source data and report the data issues periodically..

  • Ability to interpret project level requirements and develop programming specifications, as appropriate, for multiple studies.
  • Provide advanced technical expertise in conjunction with clients, and independently bring project solutions to Statistical Programming teams and department, for complex studies.
    Fulfill project responsibilities at the level of technical team lead for single complex studies or group of studies.
  • Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines.
  • Estimate programming scope of work, handle resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables.
  • Use and promote the use of established standards, SOP and standard methodologies
    Provide training and mentoring to SP team members and department staff.
  • All responsibilities are important job functions unless noted as nonessential (N).


  • You should have Masters degree in computer science or related field and relevant experience; Bachelor's degree or educational equivalent and relevant experience; or equivalent combination of education, training and experience
  • Experience in Statistical programming in SAS within the CRO/Pharmaceutical/Biotechnology/Healthcare industries
  • Experience as project 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
  • Deep knowledge of statistics, programming and/or clinical drug development process and advanced knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language
    Good organizational, social, leadership and communication skills
  • Ability to independently lead multiple tasks and projects and to delegate work to other members of the SP team
  • Excellent accuracy and attention to detail
  • Exhibit routine and occasionally complex analytical skills
  • Recognize when negotiating skills are needed and seeks assistance
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients

If the above-mentioned position doesn't match your needs, then I would suggest to contact me directly for what I have available.

Contact Details: Jamie Haerewa (Send your CV directly to my E-Mail) or give me a call on +49 (0)89 / 21093991

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