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)

• 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