CTI
CTI6mo ago
New

Clinical Research Associate II or higher for our Korean Office

South KoreaSouth Korea·Seoulmid
HealthcareClinical Researcher
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Quick Summary

Overview

About CTI CTI Clinical Trial and Consulting Services is a global, privately held,

Technical Tools
HealthcareClinical Researcher

CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com

 

Responsibilities

~1 min read
  • →Serve as main CTI contact for assigned study sites
  • →Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP
  • →Conduct or assist with study start-up activities, including feasibility, pre-study activities and site selection
  • →Collect, review and track essential/regulatory documents
  • →Participate in and complete all general and study specific training as required
  • →Participate in investigator, client and project team meetings; may include presentations
  • →Create and implement subject enrollment strategies for assigned study sites
  • →Ensure proper storage, dispensation and accountability of all Investigational Product (IP) and trial-related materials
  • →Perform site management activities and provide ongoing updates of site status to Clinical Project Manager
  • →Conduct onsite / remote monitoring and complete related activities in accordance with study specific Monitoring Plan
  • →Utilize systems and reports to track subject status, subject case report form (CRF) retrieval / source document review (SDV), regulatory documents, and IP
  • →Assist with project-specific activities as member of Project Team

 

  • 2-5 years clinical research experience as a CRA or related profession in South Korea
  • Life science background
  • Excellent knowledge in KGCP, ICH-GCP and regulatory requirements
  • Experience in Oncology or Transplant is a plus
  • Fluent (Level B2 to C1) in spoken and written language in Korean and in English
  • You need to be fully eligible to work in Korea. CTI does not offer any Sponsorship

At CTI, we recognize that our people are what make our company successful. Our work moves medicine forward.

  • Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through a dedicated training department.
  • Join an Award-Winning and Valued Team – We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering hybrid work from home opportunities. We also encourage care for the world around us through our unique CTI Cares program.
  • Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market. 

 

  • We will never communicate with you via Microsoft Teams or text message
  • We will never ask for your bank account information at any point during the recruitment process

Location & Eligibility

Where is the job
Seoul, South Korea
On-site at the office
Who can apply
KR

Listing Details

Posted
March 12, 2026
First seen
May 6, 2026
Last seen
September 27, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
9%
Scored at
May 6, 2026

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CTIClinical Research Associate II or higher for our Korean Office