Senior Statistical Programmer I

12 hours ago


Adelaide, South Australia Avance Clinical Full time

Join to apply for the Senior Statistical Programmer I role at Avance Clinical3 days ago Be among the first 25 applicantsJoin to apply for the Senior Statistical Programmer I role at Avance ClinicalWho are we?
We're Avance Clinical a Contract Research Organisation.
We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry.
We have a rich history in this area with our founding roots dating back to the 1980's.
If you already work in this industry you'll know that we are experts in our field.Who are we?
We're Avance Clinical a Contract Research Organisation.
We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry.
We have a rich history in this area with our founding roots dating back to the 1980's.
If you already work in this industry you'll know that we are experts in our field.We are looking for a Senior Statistical Programmer to be based in Adelaide.Why should you join Avance Clinical?
We appreciate that our most important asset is our people.
We offer a fun, friendly work environment and a culture that values honesty and respect.
We have a strong sense of team.
We genuinely appreciate each individual but recognise the collective when achieving success.We are committed to creating a flexible work environment for our people by supporting them to balance their work commitments and personal needs, both now and into the future.Broad PurposeThe Senior Statistical Programmer is responsible for providing clinical programming expertise in the production of tables, figures and listings for inclusion in clinical study report, creation and quality control (QC) of CDISC datasets and associated documentation, and other summaries of data collected from clinical trials.
In addition, the Statistical Programmer will contribute to the development of Avance procedures and be responsible for the management of project specific statistical programming tasks and deliverables.Core ResponsibilitiesPreparation of listings, tables and figures for clinical study reports.Creation of primary and QC SAS programs for CDISC datasets and associated documentation.Assists with the preparation of statistical analysis plans (including preparation/review of listing, table and figure shells) and randomization schedules.Liaising with Data Management team and bioanalytical laboratories regarding data



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