Principal Programmer Oncology

About the role

Overview Work as a principal programmer across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines.

What you'll do

• Program and validate datasets and SDTMs, including complex efficacy, labs, etc
• Become independent technical expert
• Program complex non efficacy outputs/ figures
• Perform Senior Review and Deliver QC of non- statistical output
• Become involved in developing the standard macro library and take responsibility to implement standard macros within a study

What you need

• VBA
• SOP writing
• SAS
• Regulatory affairs
• GCP
• B.Sc