Clinical Research Coordinator OnSite in Okinawa, Japan
Company: Arcetyp LLC
Location: National City
Posted on: April 1, 2026
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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. Services include Management & IT
Consulting, Program & Project Management, and Professional & Admin
Services. We can't sponsor H1B. We accept direct hire candidates
only, W2 employee hires. We do not accept 1099 independent
consultants. We do not accept staffing firms. We do not accept
corp-to-corp (C2C) candidates. Arcetyp LLC is looking for a
Clinical Research Coordinator . This position is onsite and located
in Okinawa, Japan. DUTIES AND 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.
EDUCATION AND YEARS OF EXPERIENCE: 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.
QUALIFICATIONS: 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 Min. Citizenship Status Required: U.S
Citizenship. Physical Requirement(s): None Location: Okinawa, Japan
COMPENSATION: Pay and benefits information for this position will
be provided to interested candidates that apply. Arcetyp offers a
package of compensation and benefits to full-time salaried
employees. Arcetyp is an Equal Opportunity Employer and we highly
value diversity of our workforce. We accept resumes from all
interested parties and consider applicants for all positions
without regard to race, color, religion, sex, national origin, age,
marital status, sexual preference, personal appearance, family
responsibility, the presence of a non-job-related medical condition
or physical disability, matriculation, political affiliation,
veteran status, or any oth er legally protected status.
Keywords: Arcetyp LLC, Encinitas , Clinical Research Coordinator OnSite in Okinawa, Japan, Administration, Clerical , National City, California
