Senior Statistical Programmer
hace 1 mes
As a Senior Statistical Programmer at Iqvia, you will be responsible for performing, planning, and coordinating complex studies involving statistical programming, testing, and documentation. You will work with internal and external clients to provide advanced technical expertise and bring project solutions to teams and departments.
You will be responsible for programming, testing, and documenting statistical programs for use in creating statistical tables, figures, and listing summaries. You will also program and plan the integration of databases from multiple studies or sources and develop and coordinate programming documentation.
Requirements include a Bachelor's or Master's degree in Computer Science, Mathematics, or equivalent, and 5+ years of experience in statistical programming within the Life-Science industry. You should have excellent knowledge of CDISC standards, SAS Base, and SAS Macros, as well as strong application development skills and a good understanding of clinical trial data.
As a technical team lead, you will directly engage with clients and coordinate tasks within a programming team. You should have in-depth knowledge of applicable clinical research regulatory requirements, such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Join Iqvia to take your skills to the next level and enjoy global exposure, a variety of therapeutic areas, and a collaborative and supportive team environment.
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