Responsibilities:

Plan and manage programming activities across multiple studies to deliver all data analysis outputs to agreed timelines and quality, (e.g., analysis datasets, tables, figures and listings for regulatory submissions and publications).

Oversee outsourced tasks to third party vendors to meet the agreed timelines, quality and budget requirements established for the project or study.

Implement data standards within a function, or therapeutic area in accordance with industry standards

Responsible for programming and QC across a study/asset including submission activities adhering to relevant SOPs / policies.

Participate in the design of other study delivery components (e.g. case report forms, study databases).

Review and input into key study documents (e.g. SAP, CRF etc).

Provide technical advice, mentoring and training as relevant.

The Senior Programmer acts as a support for GSK clinical trials, acc...