Programming Manager

About the role

Overview Work as a experienced programmer across multiple clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Line managing members of staff, contributing to management meetings.

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
• Coordinate and perform code reviews

What you need

• 3–6 years in software engineering
• VBA
• SAS
• Regulatory affairs
• GCP
• B.Sc