**GFR Senior Statistical Programmer - Based UK


Provide 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.


Perform, plan co-ordinate and implement the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal and external clients and (iii) the programming quality control checks for the source data and report the data issues periodically..

Ability to interpret project level requirements and develop programming specifications, as appropriate, for complex studies.

Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and Statistical Programming department, for complex studies.

Fulfill project responsibilities at the level of technical team lead for single complex studies or group of studies.

Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines.

Estimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables.

Use and promote the use of established standards, SOP and best practices.

Provide training and mentoring to SP team members and Statistical Programming department staff.

All responsibilities are essential job functions unless noted as nonessential (N).


Statistical programming in SAS within the CRO/Pharmaceutical/Biotechnology/Healthcare industries

SDTM and ADaM experience

Previous experience in CDARS reporting system

Experience as technical team lead directly engaging clients and coordinating tasks within a programming team

In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Knowledge of statistics, programming and/or clinical drug development process

Advanced knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language

Good organizational, interpersonal, leadership and communication skills

Ability to independently manage multiple tasks and projects

Ability to delegate work to other members of the SP team

Excellent accuracy and attention to detail

Ability to delegate work to other members of the SP team [SPM]


Masters degree in computer science or related field and 3 years relevant experience; Bachelor’s degree or educational equivalent in computer science or related field and 5 years relevant experience; or equivalent combination of education, training and experience

Back to top