Sharing a Vision to Drive Healthcare Forward
Healthcare is an industry designed to help humans. As a global community, we continuously invest and commit to advancing human health. To deliver value and real outcomes. To rise to the challenge to find the next breakthrough by making the most of increasingly limited resources.
We are inspired by the potential ...
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Senior Statistical Programmer: Real World Evidence - homebased or hybrid working
As a Senior Statistical Programmer, you will provide experienced technical expertise to develop process methodology for the department to meet internal and external clients’ needs.
You will plan and coordinate the development of integrated programming solutions, serving the full spectrum of statistical programming needs, along with providing technical expertise and leadership to the department and provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.
Acting as a lead on studies, you will directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines and support the training of new or junior team members. As well as estimating programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables.
Please apply in English
Essential Requirements:
5+ years Statistical Programming experience within the Life-Science industry
Experience in SAS® Base, and good knowledge of SAS® graph and SAS® Macros
Ability to implement more advanced statistical procedures as per specifications provided by Biostatisticians.
Excellent knowledge of CDISC standards (SDTM and ADaM)
Already possess the right to work in EMEA
Thorough understanding of relational database components and theory
Excellent application development skills
Experience as technical team lead, directly engaging clients and coordinating tasks within a programming team
Bachelors or Masters’ in Computer Science, Mathematics or equivalent
In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good Clinical Practice
(GCP) and International Conference on Harmonization (ICH) guidelines
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