Senior Statistical Programmer

Tasks

• Apply automation to improve efficiency
• Collaborate with statisticians lead programmers data managers and study leaders
• Create reliable datasets and analyses
• Deliver high quality programming outputs on schedule
• Ensure adherence to CDISC and internal standards
• Ensure audit ready documentation completeness
• Identify and communicate programming risks
• Implement statistical programming aspects of protocols
• Influence stakeholder decisions with programming expertise
• Lead clinical study programming deliverables
• Partner with contract programming providers
• Plan track and deliver programming project aspects
• Program independently using advanced techniques and macros
• Support regulatory submissions programming activities
• Write programming specifications

Perks/Benefits

• English required
• Flexible office attendance
• On site three days per week

Skills/Tech-stack

Automation | CDISC | Clinical Development | Clinical trials | Data Analysis | Programming documentation | Project Management | R | Regulatory Submissions | SAS | SAS Macros | Statistical programming