|勤務地||Japan - Tokyo|
Global biopharma company
• Support execution of RBM processes as a part of cross-functional teams spanning the R&D portfolio (all therapeutic areas and phases of development).
• Utilize analytics/visualizations to review aggregate data for the remote
assessment of Risk Indicators that identify issues and emerging risks
at the study, program, country, therapeutic and functional level, to
ensure risks are addressed consistently.
• Identify critical data issues and document findings for tracking and
Contribute to the development of or provide feedback on training
material developed to support RBM methods.
・3+ Years in drug development and/or,
・3+ Years in the field of site management, site monitoring, data management or related.
・Demonstrated ability to effectively communicate ideas/concepts and
to motivate others to accomplish challenging shared goals and objectives.
・Well-versed in analytical and conceptual capabilities
・Demonstrated ability to apply critical thinking and identify, distinguish
relative importance and be able to work through issues remotely
・Demonstrated knowledge of clinical operations, inclusive of site monitoring, management and data management
・Demonstrated knowledge of Good Clinical Practices (GCP)