Clinical Research Coordinator On Site Okinawa, Japan

Arcetyp LLC•San Diego, CA

1d•Onsite

About The Position

Arcetyp LLC is seeking a Clinical Research Coordinator to join their growing small business. This position is onsite and located in Okinawa, Japan. Arcetyp LLC provides a broad range of consulting services to US Federal Government, US Military, and Commercial clients, including Management & IT Consulting, Program & Project Management, and Professional & Admin Services. The company is looking for direct hire candidates only, W2 employee hires, and does not accept H1B sponsorship, 1099 independent consultants, staffing firms, or corp-to-corp (C2C) candidates.

Requirements

Bachelor’s Degree from an accredited college or university and a minimum experience of 2 years 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) from the Association of Clinical Research Professionals (ACRP) OR the Society of Clinical Research Associates (SoCRA).
Minimum of 2 to 4 years of monitoring experience in a clinical research environment and administrative Institutional Review Board (IRB) experience.
Possess knowledge of medical terminology and clinical monitoring process and in depth therapeutic and protocol knowledge.
Ability to communicate effectively, both orally and in writing.
Possess effective organizational and analytical skills with ability to work independently and in a team environment.
Proficiency with Windows base computer systems, including Microsoft Windows and Microsoft Office Suites program.
Candidate must possess active/current secret security clearance.
Must possess the ability to complete research subject protection training developed by the Collaborative Institutional Training Initiative (CITTI), and additional protocol specific training, as required, within one month from start date.
U.S Citizenship.

Responsibilities

Coordinates and participates in clinical research studies by performing a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data.
Coordinates and implements procedures for data collection from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources.
Assists in the determination of guidelines for the collection of clinical data or administration of clinical studies.