Perform statistical work for clinical trials and regulatory submission documents in vaccine projects
Create and manage quality of statistical analysis plans to provide statistical work for regulatory submission documents, including clinical study reports
Provide statistical advice as a statistician for development plans and protocol creation
Support programming tasks as needed
Collaborate as a member of Development Japan (DJ) utilizing communication with global teams (phone, email)
応募資格:
English proficiency (reading and writing: intermediate level, conversation: intermediate level)
TOEIC score of 600 or higher
SAS/R programming skills
Biostatistics training (BioS, etc.)
5+ years of experience in statistical work in clinical development (including creation of statistical analysis plans)
Vaccine development experience and motivation is desirable