Recruiting Information


Background of recruitment:
As a member of Roche group, generating clinical development plan (CDP) as well as organized structures enabling value maximization after market-in and medical activity-oriented highly strategic planning are prerequisites for providing innovative medicines to patients globally. To this end, individuals who can generate clinical development plan as well as design clinical study, create analysis plan, perform data analysis and discuss with Health Authority at filing and review for new medicines by statistical point of view are desired.
Type of employment Regular employees
Description of work
  • Provide statistical input to planning clinical development plan by statistical point of view
  • Design clinical study, preparing documents including statistical Analysis plan
  • Communicate with biostatistician in Roche/Genentech
  • Discuss with Health Authorities at a meeting, filing and review
Required qualifications
  • Master degree in statistics or other related science fields or equivalent knowledge and skills
  • minimum 3 years of experiences with biostatistics of clinical study in pharmaceutical industry, CRO or health authorities etc.
  • TOEIC score 730+ or equivalent English skills, and ability to communicate in English
  • Good knowledge of ICH/Health Authorities' regulations applicable to clinical study.
  • Good skills and experience of statistical programming languages, e.g. SAS
  • Good collaborative skills and ability to work cross-functional team members
Place of business Main Office (Chuo Ward, Tokyo)
Hours Flex time system (core time: 11:30–13:30)

To be decided in accordance with our criteria

Application method Please apply via the link below.
* We will not disclose any application to any third party.
* We will not use documents submitted by applicants for any purposes other than screening.
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