Key Responsibilities:
Perform, plan co-ordinate, and implement the following for complex studies:
The programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing
The programming of analysis datasets (derived datasets) and transfer files for internal and external clients
The programming quality control checks for the source data and to report the data issues periodically
Ability to interpret project level requirements and develop programming specifications, as appropriate, for complex studies.
Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams
Fulfil 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, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables
Use and promote the use of established standards, SOP and best practices
Provide training and mentoring to SP team members
Requirements:
Bachelor’s Degree in Maths, Computer science, Statistics, or related field
7+ years’ Statistical Programming experience within the Life Science Industry
Strong Efficacy experience
Advanced knowledge of statistics, programming and/or clinical drug development process
Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language
Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM)
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