We've got the best role for a Principal SAS Programmer based anywhere in the UK. Our client has offices across the UK so you have options to be office based too. You should have great project management skills as well as being an expert in clinical trials, SAS programming and statistics.

If you are at a different level, please let us know as we do have a range of roles.

THE ROLE

As a principal SAS programmer, you will hold a combined project leadership, line management (if desired) and hands-on technical programming role. Working across a range of phases and therapeutic areas, you will lead assigned studies, ensuring they are delivered to optimal quality, on time and on budget.

Key Responsibilities:

Responsibility for overall project delivery, including clinical trial reports and other regulatory submission deliverables

Project management responsibilities, including allocating staff, predicting and planning resources

Act as a study expert for multiple studies, with an ability to clarify details on analysis methods for the internal team

Advise on internal, client and CDISC data standards

Responsible for ensuring the team meets the highest quality standards, and follows the principles detailed in internal procedures

Function as a programming expert across multiple studies

Maintain a positive and engaging client relationship with regards to statistical/programming issues

Report on study progress to the management team

Mentor, train and develop direct reports

SKILLS AND EXPERIENCE REQUIRED

BSc, MSc or PhD in mathematics, science or IT related discipline

Experience working within a clinical trials environment (CRO, pharma or academia)

Substantial experience performing statistical analysis using SAS

CDISC (SDTM and ADaM) experience

Proven project leadership experience

Previous line management / mentoring experience preferred (not essential)

Excellent written and verbal communication skills

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