Join a fast-paced and agile global team with direct strategic impact on drug development, empowered to innovate and experiment
Job Summary
Join a fast-paced and agile global team with direct strategic impact on drug development, empowered to innovate and experiment.
As a Senior Statistical Programmer, you are responsible for leading programming deliverables of a clinical study or a small to medium sized clinical project, ensuring quality and timeliness.
This role offers an opportunity to play a pivotal role in making a positive impact on changing patients’ lives within a vibrant and collaborative office environment.
Matching Summary
Join a fast-paced and agile global team with direct strategic impact on drug development, empowered to innovate and experiment.
Skills & Requirements
Must-have
SAS programming and SAS macros
CDISC industry standards
clinical drug development process
programming deliverables quality and timeliness
independent programming tasks
Nice-to-have
innovate and experiment
collaborative work environment
diverse and inclusive team
fresh thinking to the table
technical initiatives
Key Requirements
Degree in Mathematics, Statistics, Computer Science, Life Science, or equivalent
Excellent programming skills in SAS (or R)
Proficient knowledge of clinical development process and industry standards
Ability to apply programming knowledge to problem solving
Ability to manage relevant documentation
Ability to influence relevant stakeholders
Current knowledge of technical and regulatory requirements