[Innovative Medicine] R&D, Experienced I Stat Programmer, Clinical & Statistical Programming Japan, Global Development

Tasks

• Contribute to process improvement projects
• Create and deliver CDISC compliant data packages
• Create reviewer guides
• Design and develop programs for clinical research analysis and reporting
• Develop clinical programming deliverables
• Ensure compliance with company and departmental processes and training
• Review and provide input for project requirements and documentation
• Support submission activities for clinical trials
• Verify programming and reporting activities

Perks/Benefits

• Diversity and respect
• Inclusive work environment
• Training and development

Skills/Tech-stack

CDISC | Clinical Practice | Clinical trials | Data Privacy | Data Quality | Data Structures | Good Clinical Practice | Python | R | Report Writing | SAS | Statistical Analysis