【求人No NJB2273386】
As a CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets. You will have the opportunity to work on clinical studies in various therapeutic areas and indications while maintaining the highest quality standards in the industry. This function operates at site and country level and can be assigned to projects as monitor or lead monitor.
| 職務経験 | 無し |
| キャリアレベル | 中途経験者レベル |
| 英語レベル | ビジネス会話レベル |
| 日本語レベル | ネイティブ |
| 最終学歴 | 大学卒： 学士号 |
| 現在のビザ | 日本での就労許可が必要です |
College/University degree in Life Sciences Pharmacy RN or an equivalent combination of education training experience
At least 3 years’ site monitoring experience at a CRA II or equivalent qualification level in Japan
Experience in all types of monitoring visits in Phase II and/or III
Experience in feasibility assessment and study set up process is preferable
Therapeutic area experience in Oncology /Hematology /Gastroenterology （IBD） /Infectious Diseases /Neurology/Renal is a plus
Full working proficiency in Japanese and Intermediate English
PC skills to be able to work with MS Word Excel and PowerPoint
Ability to plan multitask and work in a dynamic team environment
Communication collaboration and problem solving skills
Ability to travel up to 30% to 40%
正社員
給与600万円 ~ 1000万円
勤務時間09:00 ～ 18:00
休日・休暇【有給休暇】初年度 最大10日（入社月によって異なる） 【休日】完全週休二日制 土 日 祝日 年末年始
業種CRO
外資系企業
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