Clinical Development (Clinical Safety Scientist)
- Background of recruitment：
- Safety issues, identification of adverse events, and signal detection are getting more and more important with respect to patient protection and ICH harmonization. Since we are implementing simultaneous global clinical trials, a candidate with experience in evaluation of safety data for non-clincial and clinical development is required. In addition, a candidate with experience of product value maximaization and clinical development strategy from a safety perspective is sought.
|Type of employment||Regular employee|
|Description of work||As a leader (or a deputy-leader) in the safety management group of our Clinical Development Division, the candidate will perform detection of safety signals and establish risk management actions for products, define benefit-risk balance, and be an author of periodic reports such as DSUR and related clinical development documents (protocols, IB, etc). In addition, the candidate will play a major role in compiling core safety information of products. Management of several direct reports is also expected.|
|Required qualifications||・Bachelor's degree as a minimum (faculty of medicine, dentistry, pharmacology, or veterinary medicine)
・2-years or more experience of safety signal detection and risk management in clinical development / 2-years or more experience of clinical science (either of above)
・Experience of safety risk evaluation of non-clinical data is desirable
・English language level suitable for communication with overseas affiliates (e.g. TOEIC score 700+).
|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.
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.