CareerCross uses cookies to enhance your experience on our websites. If you continue to view our sites without changing your browser settings, then it is assumed that we have your consent to collect and utilise your cookies. If you do not want to give us your consent, then please change the cookie settings on your browser. Please refer to our privacy policy for more information.
CareerCross uses cookies to enhance your experience on our websites. If you continue to view our sites without changing your browser settings, then it is assumed that we have your consent to collect and utilise your cookies. If you do not want to give us your consent, then please change the cookie settings on your browser. Please refer to our privacy policy for more information.
| Hiring Company | CSLベーリング株式会社 |
| Location | Tokyo - 23 Wards |
| Job Type | Permanent Full-time |
| Salary | 6.5 million yen ~ 10 million yen |
【求人No NJB2361432】
■Responsibilities:
Handling and assist management of safety related information of investigational products in accordance with GCP and support development tasks.・
Handling and assist management of safety related information of marketed products in accordance with GVP
Planning and implementation of measures for securing safety such as information providing/disseminating and assist management of those tasks
Implement and assist management・ of other GVP/GCP activities・ (archiving SOP management Training Outsourcing etc.)
Managing GVP/GPSP SOPs/WIs/other documents in Japan
Managing Vender including sign GVP agreement and PVA
Managing Organized Data Collection System (ODCS)
■Main Responsibilities and Accountabilities
1. Implement and assist management of collecting and evaluating safety management information such as AEs or infection cases and reporting to authorities. (Evaluating safety management information preparing reports submitting to authorities and archiving records)
2. Implement and assist management of exchanging safety information with relevant global organization and business partners.
3. Implement and assist management of preparing periodic reports and submitting them to authorities.
4. Planning and implementation of measures for securing safety such as information providing/disseminating and assist management of those tasks
5. Implement and assist management of creating and updating CTD1.11(J RMP) in the safety part receiving global approval and answering PMDA inquiries.
6. Implement and assist management of other GVP/GCP activities (archiving SOP management Training Outsourcing etc.)
7. From safety perspective join JPT and support development tasks.
8.・Implementing and managing procedure documents according to GVP/GPSP and confirming global SOPs/WIs/other documents (SOP management etc.)
9.・Managing Organized Data Collection System (ODCS) including the website in Japan according to GSPV standards
10.・Coordinating PVA signing in Japan in cooperation with GSPV
| Minimum Experience Level | No experience |
| Career Level | Mid Career |
| Minimum English Level | Business Level |
| Minimum Japanese Level | Native |
| Minimum Education Level | Bachelor's Degree |
| Visa Status | Permission to work in Japan required |
■Job Qualifications and Experience Requirements
◇Education
Bachelor’s degree science is preferable;
◇Experience
Experience of PV activities under GCP and/or GVP; 3 years or more experience of safety is preferable.
◇Competencies
・knowledge of GCP/GVP/GPSP related laws and regulations in Japan
・Proficiency in written and spoken Japanese
・Good communication skills in English
・Good communication skills both internally and externally
・Problem solving / logical thinking
| Job Type | Permanent Full-time |
| Salary | 6.5 million yen ~ 10 million yen |
| Work Hours | 08:45 ~ 17:30 |
| Holidays | 【有給休暇】初年度 16日 1か月目から(入社月によって異なります) 【休日】週休二日制 土 日 祝日 夏季休暇 年末年始 年… |
| Industry | Pharmaceutical |
| Company Type | International Company |