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.
Maintains well organized, complete, and up-to-date project documentation, testing, and verification/quality control documents and programs ensuring inspection readiness.
Develops specifications for datasets and outputs of any complexity according to statistical or sponsor requirements.
Acts as the lead statistical programmer. Directs the programming activities of other programming personnel and monitors progress on programming deliverables.

Undergraduate degree, preferably in a scientific or statistical discipline;
Extensive programming experience in SAS or other required software, preferably in a clinical trial environment;
Knowledge and experience in the use of CDISC Standards for regulatory agency requirements;
Experience in submissions to a regulatory agency preferred.
Experience in mentoring others in clinical trial process and CDISC Standards.
Excellent written and verbal communication skills.
Ability to read, write, speak and understand English.

We are passionate about developing our people, through career development and progression;
supportive and engaged line management;
technical and therapeutic area training;
peer recognition and total rewards program.
We are committed to building an inclusive culture – where you can authentically be yourself.

Principal Statistical Programmer – Clinical Pharmacology

Key skills