This role is responsible for leading programming deliverables of a clinical study or small to medium sized clinical project with high quality and timeliness
Job Summary
This role is responsible for leading programming deliverables of a clinical study or small to medium sized clinical project with high quality and timeliness.
The successful candidate will work within an agile global team at AstraZeneca CVRM Biometrics to impact drug development programs.
Candidates must possess excellent programming skills in SAS or R along with thorough industry knowledge of clinical development processes.
Matching Summary
This role is responsible for leading programming deliverables of a clinical study or small to medium sized clinical project with high quality and timeliness.
Skills & Requirements
Must-have
Excellent SAS programming skills
Proficient knowledge of CDISC standards
Experience in clinical drug development
Nice-to-have
Broad experience across therapeutic areas
Experience in regulatory submissions
Ability to lead cross-functional teams
Key Requirements
Degree in Mathematics, Statistics, Computer Science, or Life Science
Current knowledge of technical and regulatory requirements
Ability to manage relevant documentation independently