Associate Director, Statistical Programming (LM)
Tasks
- Act as technical subject matter expert
- Deliver clinical study statistical programming
- Develop data standards and automation approaches
- Drive continuous improvement and best practices
- Lead and manage programming team
- Lead statistical programming protocol implementation
- Manage clinical programming compliance and quality
- Manage external partners and CROs
- Provide training and mentorship
- Recruit and develop team talent
Perks/Benefits
Skills/Tech-stack
Automation | CDISC | Clinical trial | Data Standards | R | Risk Management | SAS | SAS Macros
Education
Bachelor of Engineering | Bachelor of Science | Master of Science | PhD
Related jobs
-
Associate Director - Operational Effectiveness PLN 180K-383KAgile | Analytics | Artificial Intelligence | Automation | Business caseMid-level Full TimeWarsaw, Poland7d ago
-
Associate Biostatistician PLN 230K-380KClinical Trial Design | Clinical trial | Quality Control | R | SASMid-level Full TimePoland, Warsaw R8d ago
-
Associate Director, Biostatistics PLN 430K-521KAnalysis planning | Biostatistics | Clinical Trial Design | Clinical study reports | Clinical trialMid-level Full TimeWarsaw, Poland15d ago