Description
We are seeking an experienced CRA (Clinical Research Associate) to join our team in Tokyo, Japan. As a CRA, you will be responsible for performing site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.
Responsibilities:
- Conduct monitoring activities according to the Clinical Monitoring Plan (CMP) and study protocol
- Obtain case report forms (CRFs) within the specified timeframe and perform Source Data Verification (SDV)
- Create monitoring reports
- Identify and report adverse events, including serious adverse events
Requirements:
- Completed GCP training
- At least 2 years of experience as a CRA under GCP
- Fluent in Japanese
- Ability to visit sites individually
Preferred qualifications:
- Experience in oncology and/or CNS therapeutic areas
- Global project experience
- Experience working in university hospitals or oncology hospitals
- Mentorship experience for new clinical staff
Benefits:
- Competitive salary
- Comprehensive benefits package, including social insurance and IQVIA's unique benefits
- Opportunities for career growth and professional development
- Flexible working arrangements, including remote work options
Working conditions:
- Full-time employment
- Standard working hours: 9:00-17:30
- Expected overtime: 10-20 hours per month