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.
Follows 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.
Manages scheduling and time constraints across multiple projects at a time, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload.

5 to 8 years of experience working on end to end stat programming activities with ADAM / TFL's & SDTM
Exposure on Early Phase studies / PK PD trials is preferred
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.

passionate about developing our people, through career development and progression
supportive and engaged line management
technical and therapeutic area training
peer recognition
total rewards program
committed to building an inclusive culture
driven to deliver

Senior Statistical Programmer – Clinical Pharmacology

Key skills