[Osaka & Tokyo] Clinical Research Associate (CRA) in Operation

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Job details

Company overview

In the global CRO market, it is a Japanese subsidiary of a top-level drug development contract entrusted organization.

Responsibilities

• MANAGE / MONITOR THE PROGRESS OF YOUR TRIAL ON-SITE OR OFF-SITE, AND CONDUCT, RECORD, AND REPORT YOUR TRIAL IN ACCORDANCE WITH CLINICAL TRIAL PROTOCOL, SOPS, ICH / J-GCP, AND OTHER APPLICABLE LAWS AND REGULATIONS. GUARANTEE THAT YOU ARE
• RESPONSIBLE FOR CONTRACT NEGOTIATIONS AND CONCLUSIONS WITH MEDICAL INSTITUTIONS
• WORK CLOSELY WITH OTHER CLINICAL TEAM MEMBERS TO TIMELY RESOLVE ANY CLINICAL TRIAL ISSUES THAT ARISE
• INEXPERIENCED GIVE APPROPRIATE GUIDANCE TO MEMBERS AND CONTRIBUTE TO THEIR GROWTH

Requirements

EDUCATIONAL BACKGROUND:

• UNIVERSITY GRADUATE OR ABOVE, OR MEDICAL (NURSE, CLINICAL LABORATORY TECHNICIAN, ETC.)

LANGUAGE:

• JAPANESE NATIVE
• ENGLISH - CONVERSATION 
• ENGLISH SKILLS THAT DO NOT INTERFERE WITH WORK (READING COMPREHENSION, WRITING DOCUMENTS / EMAILS, ETC.)

WORK EXPERIENCE:

• TWO YEARS OR MORE OF CRA EXPERIENCE AT A PHARMACEUTICAL COMPANY OR CRO
• IN TEACHING AND TRAINING OTHER CRA
• THE SPIRIT OF BEING ABLE TO TAKE ON NEW CHALLENGES
• HUMANITY OF BEING ABLE TO WORK ENTHUSIASTICALLY ON NEW DRUG DEVELOPMENT WORK
• SPECIALTY BACKED BY WORK EXPERIENCE SUCH AS CLINICAL DEVELOPMENT
• TRUST WITH MEDICAL INSTITUTION PERSONNEL, ETC. HUMAN POWER TO BUILD RELATIONSHIPS

Salary

9 - 14 million yen

Location

Other