Senior Statistical Programmer at Worldwide Clinical Trials
VICTORIA, Victoria, Australia -
Full Time


Start Date

Immediate

Expiry Date

29 Dec, 26

Salary

54000.0

Posted On

30 Sep, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Hospitals & Health Systems

Description

This position provides high quality statistical programming deliverables for global stakeholders in Early Development Statistics and/or PK/PD Modeling and Simulation spanning all our Company's therapeutic areas. The senior statistical programmer will gather and interpret user requirements for programming requests, retrieve required data, transform data into analysis/modeling datasets, and develop tables, listings and figures according to statistical/modeling analysis plan. The senior programmer will partner with stakeholders to solve problems; reduce the amount of programming tasks being completed by stakeholders to facilitate an increase in efficiency and compliance for the analyses. The senior programmer will also write programs to analyze data with statistical methods which are not currently available through commercial software packages. The programmer will be a key collaborator with statisticians, pharmacokinetic (PK) modelers, and other project stakeholders.

Responsibilities

Programmatically develop, validate and maintain complex datasets, tables, listings, and figuresProvide technical consultation and analytical support to statisticians and PK modelers for exploratory and unplanned statistical analysesPrepare compliant programming code for regulatory submissions including analysis datasets, tables, listings, figures and associated documentationEnsure programmatic traceability from data source to analysis / modeling resultSupport the development of programming standards to enable efficient and high quality production of programming deliverablesEducation and Minimum Requirement:BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5-9 years SAS/R programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3-7 years SAS/R programming experience in a clinical trial environmentDepartment Required Skills and Experience:Effective interpersonal skills and ability to negotiate and collaborate effectivelyEffective written, oral, and presentation skillsEffective knowledge and experience in developing analysis and reporting deliverables for research and development projects (data, analyses, tables, graphics, listings)A project leader; completes tasks independently at a project level; ability to collaborate with key stakeholdersSpecific Required Skills and Experience:Experience in CDISC SDTM and ADaM standardsSignificant SAS or R programming experience for data manipulation, analysis and reportingDesigns and develops complex programming algorithmsAbility to comprehend analysis plans which may describe methodology to be programmed; understanding of statistical terminology and concepts; Implements statistical methods not currently available through commercial software packagesDemonstrated ability to work in an exploratory environment, handling non-standard data in a variety of formats with minimal requirements; knowledge of pharmaceutical development processes



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