Permanent Statistical Programmer Job Vacancies

2 of 2 Permanent Statistical Programmer Jobs

Senior Statistical Programmer

United Kingdom
IQVIA LLC
Senior Statistical Programmer page is loaded Senior Statistical Programmerlocations: Reading, Berkshire, United Kingdomtime type: Full timeposted on: Posted Todaytime left to apply: End Date: September 30, 2025 (18 days left to apply)job requisition id: RProvide experienced technical expertise to develop process methodology for department to meet internal and external clients' needs. Plan and coordinate the development … of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.Essential Functions• Perform, plan and co-ordinate the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use … in creating statistical tables, figures, and listing summaries and (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks. • Program and plan the integration of databases from multiple studies or sources. • Develop and co-ordinate programming documentation including plans and specifications More ❯
Employment Type: Permanent
Salary: GBP Annual
Posted:

Principal Statistical Programmer

United Kingdom
Tech Observer
Tech Observer is hiring Senior Statistical Programmers and Principal Programmers in UK and Europe on FSP. Job Responsibilities (But not limited to) Carry out all activities according to Tech Observer SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP). Ensure adherence to programming guidelines. Implement and follow the latest versions of … CDISC, FDA Guidelines, GCP and other industry standards; Participate in and co-ordinate the Statistical Programming review of Case Report Forms (CRFs), annotated CRFs, database structures and study related documentation (e.g. data validation guidelines). Review and interpret Report and Analysis Plans and provide comments for assigned projects. Develop and review SAS programs and output for the management of … clinical trial data, the tabulation of data, preparation of patient data listings, graphical output, and creation of derived datasets and statistical analysis of data as specified in the Statistical or Report Analysis Plans. Develop SAS programs for ad hoc tables and listings. Write, modify, and maintain programs that produce diagnostics and listing for data review in support of More ❯
Posted:
Statistical Programmer
Median
£55,000