Duties: Works to ensure that outputs meet quality standards and project requirements; Performs validation programming and works with other Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings; Keeps project team members informed of programming progress and issues requiring their attention; Follow applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH); Maintains well organized, complete, and up-to-date project documentation, testing, and verification/quality control documents and programs ensuring inspection readiness
Requirements: Undergraduate degree, preferably in a scientific or statistical discipline; in lieu of degree, an equivalent combination of education and demonstrated programming experience; Extensive programming experience in SAS or other required software, preferably in a clinical trial environment; Excellent written and verbal communication skills; Ability to read, write, speak and understand English

Duties: Uses SAS or other software to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications; Works to ensure that outputs meet quality standards and project requirements; Performs validation programming and works with other Statistical Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings; Keeps project team members informed of programming progress and issues requiring their attention; Follows applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH)
Requirements: Undergraduate Degree, preferably in a scientific or statistical discipline; In lieu of degree, an equivalent combination of education and demonstrated programming experience; Proficiency in programming in SAS or other required software, preferably in a clinical trial environment; Excellent written and verbal communication skills; Ability to read, write, speak, and understand English

Duties: Uses SAS or other software to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications; Works to ensure that outputs meet quality standards and project requirements; Performs validation programming and works with other Statistical Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings
Requirements: Undergraduate Degree, preferably in a scientific or statistical discipline; In lieu of degree, an equivalent combination of education and demonstrated programming experience; Proficiency in programming in SAS or other required software, preferably in a clinical trial environment; Excellent written and verbal communication skills; Ability to read, write, speak, and understand English

Duties: Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications; Works to ensure that outputs meet quality standards and project requirements; Performs validation programming and works with other Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings; Keeps project team members informed of programming progress and issues requiring their attention
Requirements: Min Five (5) years’ experience in Clinnical SAS programming in a relevant clinical trial environment; Proven ability to meet deadlines; Good proficiency in SDTM, ADaM, TFLs