A European biotechnology company, specializing in creation and development of differentiated antibody therapeutics for treatment of cancer.
Performing preliminary and exploratory data analyses clinical trials.
Lead and support regulatory submission documents such as briefing documents and relevant clinical modules in J-CTD.
Collaborate cross-functionally with other R&D functions both at local and global level for clinical projects related to Japan development.
Overseeing and developing clinical projects.
A BSc or MSc level preferably within the medical, biological, pharmaceutical science or equivalent discipline
Minimum of 8 years of experience monitoring clinical trials
Business level English (and native level Japanese, reading & writing)
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