Clinical Research Coordinator Onsite Okinawa, Japan

Posted Yesterday
Be an Early Applicant
San Diego, CA, USA
In-Office
Junior
Information Technology • Professional Services • Consulting
The Role
Coordinates clinical research studies, including collecting, compiling, documenting, and analyzing clinical data from medical records, interviews, questionnaires, diagnostic tests, and other sources. Supports clinical study procedures, data-collection guidelines, monitoring activities, and Institutional Review Board administration. Requires knowledge of medical terminology, therapeutic areas, research protocols, clinical monitoring, and research subject protection training.
Summary Generated by Built In

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 other legally protected status.

Skills Required

  • Bachelor's degree from an accredited college or university
  • At least 2 years of Clinical Research Coordinator experience within the past five years, or current CCTI, CCRC, or CCRP certification
  • 2 to 4 years of clinical research monitoring experience
  • Administrative Institutional Review Board experience
  • Knowledge of medical terminology and clinical monitoring processes
  • In-depth therapeutic and clinical protocol knowledge
  • Effective oral and written communication skills
  • Organizational and analytical skills, with ability to work independently and in a team
  • Proficiency with Microsoft Windows and Microsoft Office
  • Active and current Secret security clearance
  • U.S. citizenship
  • Ability to complete CITI research subject protection and protocol-specific training within one month of starting
  • W2 direct-hire employment; no 1099, staffing-firm, or C2C arrangements
Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
10 Employees

What We Do

Arcetyp LLC is a growing small business that provides a broad range of growth and consulting services to the US Federal Government, US Military, and commercial clients. Their core offerings include Management and IT Consulting, Program and Project Management, and Professional and Administrative Services, specifically supporting businesses within the US government contracting industry.

Similar Jobs

Tapestry - Coach and Kate Spade Logo Tapestry - Coach and Kate Spade

Temporary Sales Support Associate

eCommerce • Fashion • Retail • Sales • Wearables • Design
Hybrid
Montebello, CA, USA
16000 Employees
15-20 Hourly

Boeing Logo Boeing

ASIC / FPGA Design Verification Engineer - (Associate or Experienced)

Aerospace • Information Technology • Software • Cybersecurity • Design • Defense • Manufacturing
In-Office
El Segundo, CA, USA
170000 Employees
99K-162K Annually

Boeing Logo Boeing

Design Engineer

Aerospace • Information Technology • Software • Cybersecurity • Design • Defense • Manufacturing
In-Office
El Segundo, CA, USA
170000 Employees
99K-162K Annually

Boeing Logo Boeing

Design Engineer

Aerospace • Information Technology • Software • Cybersecurity • Design • Defense • Manufacturing
In-Office
El Segundo, CA, USA
170000 Employees
146K-223K Annually

Similar Companies Hiring

Standard Template Labs Thumbnail
Artificial Intelligence • Information Technology • Software
New York, NY
25 Employees
NODA AI Thumbnail
Artificial Intelligence • Information Technology • Software • Cybersecurity
Sydney, AU
54 Employees
Golden Pet Brands Thumbnail
Digital Media • eCommerce • Information Technology • Marketing Tech • Pet • Retail • Social Media
El Segundo, California
178 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account