As a Statistical Programmer you will be joining the world’s largest most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing:

• Complete programming activities under supervision
• Take responsibility for timely completion of all assigned development task
• Understand and apply a basic knowledge of industry standards
• Identify and begin to interpret problems in processes/results and communicate them to supervisor/manager
• Develop understanding of all applicable policies and procedures of GSK
• Execute assigned tasks with high quality, integrity and attention to detail (with some supervision)
• Perform Quality Control (QC) of own work independently
• Keep manager/supervisor informed of progress and activities; escalates issues as appropriate
• Works effectively and collaboratively within own team

You are:

• Able to lead studies under supervision.
• Able to demonstrate strong programming and domain expertise.
• Able to execute a wide range of programming activities with minimal supervision.
• Able to identify gaps in current programming best practices and offer suggestions for improvement.
• Minimum 3 years' experience within Statistical Programming in a clinical environment.