Clinical Research Coordinator in Okinawa, Japan - San Diego - Arcetyp LLC

Description

Job Description

Arcetyp LLC is a growing small business that provides a broad range of consulting services to US Federal Government, US Military, and Commercial clients.

We provide Management & IT Consulting, Program & Project Management, and Professional & Admin Services.

This role will lead business development activities for a small government contracting firm focused on IT Services and Cyber Security for clients in Civil and DoD markets.

Arcetyp LLC requires an experienced Clinical Research Coordinator responsible for:

• Coordinates and participates in clinical research studies by performing complex activities involved in data collection and analysis.
• Coordinates and implements procedures for data collection from various sources.
• Assists in determining guidelines for the collection of clinical data or administration of clinical studies.

To be successful in this position, you must have:

• Bachelor's Degree from an accredited college or university and minimum 2 years experience as a Clinical Research Coordinator within the past five years OR current certification as a Certified Clinical Trial Investigator (CCTI), Certified Clinical Research Coordinator (CCRC), OR Certified Clinical Research Professional (CCRP).
• Minimum of 2 to 4 years monitoring experience in a clinical research environment and administrative Institutional Review Board (IRB) experience.

You should possess:

• Knowledge of medical terminology and clinical monitoring process.
• Effective communication skills.
• Organizational and analytical skills with ability to work independently and in a team environment.
• Proficiency with Windows base computer systems, including Microsoft Office Suites program.
• Active/current secret security clearance.

Requirements: U.S. Citizenship.

Location: Okinawa, Japan.

Salary: $$$$$$.