Clinical Research Coordinator On Site - Okinawa, Japan
On-site · Okinawa, Japan
Okinawa, JapanOn-siteFull TimeMid LevelBachelors DegreeUnknown
Type
Full Time
Level
Mid Level
Education
Bachelors Degree
Company size
Unknown
Job Summary
On-site Clinical Research Coordinator in Okinawa, Japan, coordinating and participating in clinical studies by collecting, compiling, documenting, and analyzing data; coordinating data collection from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources; assisting in determining data collection guidelines and administration of studies.
Required Qualifications
- Bachelor’s Degree or higher
- Minimum 2 years experience as a Clinical Research Coordinator within past five years OR current certification as CCTI/CCRC/CCRP from ACRP or SoCRA
- Minimum 2-4 years of monitoring experience in a clinical research environment and IRB experience
- Knowledge of medical terminology and clinical monitoring process
- Effective communication skills (oral and written)
- Organizational and analytical skills; ability to work independently and in a team
- Proficiency with Windows and Microsoft Office Suites
- Active/current secret security clearance
- CITI training completion within one month of start date
- U.S. Citizenship required
Additional Requirements
- No H1B sponsorship available
- On-site only in Okinawa, Japan
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