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

Tasks

• Collaborate with cross-functional teams
• Create verify and deliver CDISC compliant data packages
• Create verify and deliver reviewer guides
• Design and develop programs for clinical research analysis
• Develop clinical programming deliverables
• Ensure compliance with company and departmental training
• Follow departmental processes and procedures
• Review project requirements and documentation
• Support trial data submission activities
• Verify programming and reporting activities

Perks/Benefits

• N/A

Skills/Tech-stack

Analysis systems | Biostatistics | CDISC | Clinical Practice | Clinical trials | Data Modeling | Data Structures | Good Clinical Practice | ICH GCP | Python | R | SAS | Statistical Analysis | Statistical Analysis Systems