Staff
| 常勤医師 | 降旗謙一 （慶応大学医学部卒） |
|---|---|
| 非常勤医師 | 加野象次郎 （慶応大学医学部卒） |
| 藤野忠彦 （慶応大学医学部卒） | |
| 菊池正夫 （慶応大学医学部卒） | |
| 村瀬忠 （慶応大学医学部卒） | |
| 顧問医師 | 加藤隆一 （慶応大学医学部名誉教授） |
| 川合眞一 （東邦大学医学部教授、日本臨床薬理学会理事長） | |
| Competent IRB (Institutional Review Board) | IRB is a body dedicated to reviewing a clinical trial protocol from the standpoint of an outsider, to find whether it is ethically and scientifically adequate. |
| Experienced Staff |
Principal Investigator (graduate of Keio University)
4 Investigators/Co-Investigators (same as above ) 2 Consulting physicians 3 permanent nurses + 30 part-time nurses 1 permanent pharmacist + 3 part-time pharmacists 1 lab technician + 5 part-time technicians Recruitment team (1 Japanese + 1 American) 2 clerks |
Message from pharmacist leader, Mr. Sugaya
I am responsible for IP storage/control/withdrawal in P-one Clinic. We are doing our best to store IPs by providing adequate facilities and making an effort to deliver the IPs in a safe and effective manner. We ensure the quality of clinical trials by placing strict controls on IPs. Furthermore, we, all the staff members of our Pharmaceutical department, are working diligently every day, and we know that this helps us contribute to the improvement of new drug development.
Message from lab leader, Mr. Oogoe
We run a clinical trial site, conducting especially Phase I studies. In order for us, lab technicians, to carry out higher quality operations, we try to fulfill our responsibilities and mission by maintaining the expertise of our respective department. I provide elaborate guidance to staff members on protocols of clinical trials, in close cooperation with each department. This allows us to conduct clinical trials of excellent quality. We consider a clinical trial to be a product of sharing accurate information promptly among physicians and staff members, and with that, we can develop a product more effectively.
Message from Nurses’ department
We, trial nurses, work by making the safety and health of subjects a top priority, because our subjects hope to be of service to new drug development. When we contract a clinical trial, we designate a chief nurse responsible for carrying out the main works of both inpatient and outpatient parts of the said study. The preliminary works are to make out notes and precautions based upon a given protocol as well as briefing papers on a hospitalized life, lab test, etc. and to order appropriate meals in accordance with the said protocol. Then, we will conduct the study according to the fixed test items and timetable of which the main works are to collect blood, measure vital signs and run an ECG.
We, three permanent nurses cooperate and work together with physicians, co-medical staff members and part-time nurses in carrying out clinical trials smoothly without any problem. Of course, our services contents are different from the ones of nurses working in general hospitals. Our mission is to continue to contribute to society and new drug development for a great number of patients.