Associate Statistical Programmer

Responsible for providing a statistical analysis service and SAS programming support in terms of table production for all clinical studies as required.

– Duties and Responsibilities:

– Statistical analysis of clinical trial data using basic methodology, under the direction of senior Statistical staff.
– Production of data tables and graphs to the required specification for clinical, pharmacokinetic and statistics reports.
– Generation of randomization schedules from provided specifications.
– Maintain project administration files with regard to all documents produced by Biostatistics, including associated review, QC and project tracking information and internal and external communications.
– Provide statistical support to SAS Programmers.
– SAS programming and related activities for the presentation and analysis of clinical trial data.
– Liaison with internal clients, as required, with regards to the requirements for analysis, tables and graphs.
– May perform QC of data displays for secondary efficacy and safety variables.
– Display interpersonal and effective communication skills. Co-operative and team orientated.
– Assure quality of personal work.
– Promoting a professional attitude at all times both internally and externally and dressing accordingly in an appropriate manner.
– Performs any other duties as assigned.
– BSc in a computing, life science, mathematical or statistical subject or attending school to receive a degree
– 0-6 months programming experience using SAS; Knowledge of fundamental principles of programming and program development (no SAS experience is also applicable)
– Have a good knowledge of at least 1 language: R, Phyton or SQL
– English level – Intermediate or above
– Alternative academic qualification or experience are assessed to ensure equivalent background
– Good organizational skills and the ability to prioritize tasks
– Self-motivation
– Good time management skills