Onsite Clinical Research Coordinator - Okinawa

arcetyp; San Diego (CA); On-site; USD 52,000 - 78,000; Full time

Job summary

Arcetyp LLC in Okinawa, Japan is seeking a Clinical Research Coordinator to support clinical studies for government and commercial clients. This onsite role requires a U.S. citizenship and a valid secret security clearance.

You will coordinate data collection from patient records, questionnaires, and tests, ensure documentation accuracy, and assist in monitoring and IRB procedures. Minimum 2 years CRC experience or CCTI/CCRC/CCRP certification, plus Bachelor’s degree, strong communication and IT

Qualifications

• Bachelor’s degree in a relevant field and at least 2 years as a Clinical Research Coordinator within the past five years.
• Current certification as a Certified Clinical Trial Investigator (CCTI), Certified Clinical Research Coordinator (CCRC), OR Certified Clinical Research Professional (CCRP) from ACRP or SoCRA.
• Minimum of 2 to 4 years of monitoring experience in a clinical research environment and IRB administration experience.

Responsibilities

• Coordinates and participates in clinical studies by performing data collection, documentation, and analysis.
• Coordinates data collection from patient charts, medical records, interviews, questionnaires, diagnostic tests, and other sources.
• Assists in establishing guidelines for data collection and administration of clinical studies.

Skills

Medical terminology

Clinical monitoring

Communication skills

Organizational skills

Analytical skills

Windows

Microsoft Office

Security clearance (secret)

CITI/CITI training (training)

Education

Bachelor’s Degree

Certification: CCTI/CCRC/CCRP or SoCRA/ACRP

Job description

Arcetyp LLC in Okinawa, Japan is seeking a Clinical Research Coordinator to support clinical studies for government and commercial clients. This onsite role requires a U.S. citizenship and a valid secret security clearance.

You will coordinate data collection from patient records, questionnaires, and tests, ensure documentation accuracy, and assist in monitoring and IRB procedures. Minimum 2 years CRC experience or CCTI/CCRC/CCRP certification, plus Bachelor’s degree, strong communication and IT