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CTA

Overview

CTA - Home-based, Seoul, South Korea

 

As a (CTA) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Responsibilities

What you will be doing:

  • Trial Master File: Setup and maintain the site level TMF/eTMF, coordinate on document collection, uploading into SP/eTMF, check the document completeness and provide TMF/eTMF QC if required
  • EC Submission: Coordinate on EC submission dossier and site start up preparation, EC fee application and tracking
  • Tracker/Metrics Report: Collect and update study trackers/metrics report for site level if needed
  • Site Contract and Payment: Assist in contract signature Assist in site level payment initiative and payment & invoice tracking
  • Site Materials and Equipment: Distribute site materials and equipment, document printing, shipment and other administrative
  • Administrative: Business & Dept. office Admin support if required

 

 

#LI-remote

#LI-SO1

Qualifications

You are:

  • +2 yr CTA experience in CRO/Pharmaceutical Companies
  • Oncology CRC background is preferrable
  • Excellence in communications skills
  • Good Command of English
  • Home-based

What ICON can offer you:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefitsAt ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodationsInterested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

What You Should Know About CTA, Pharmaceutical Research Associates, Inc

Are you ready to take your career to the next level as a Clinical Trial Associate (CTA) at ICON? We are the world’s largest and most comprehensive clinical research organization, driven by advanced healthcare intelligence. As a CTA, you will play a pivotal role in the management of clinical trials from the comfort of your home in Seoul, South Korea. Your responsibilities will include setting up and maintaining the Trial Master File, coordinating essential documentation, and ensuring everything is in place for smooth EC submissions. You will also be responsible for collecting and updating study trackers and metrics reports, assisting with site contract signatures, and managing payment initiatives. This role is perfect for someone with over two years of CTA experience in CRO or pharmaceutical companies, particularly if you have a background in oncology. We value strong communication skills and a good command of the English language. Join ICON, where we prioritize the welfare and development of our team. You’ll enjoy competitive salary packages, extensive health insurance options, and various benefits focused on your work-life balance. We celebrate diversity and are committed to creating an inclusive environment where everyone can thrive. So if you are looking for an exciting role that combines your passion for clinical research with the flexibility of working from home, we want to hear from you!

Frequently Asked Questions (FAQs) for CTA Role at Pharmaceutical Research Associates, Inc
What qualifications do I need to become a Clinical Trial Associate (CTA) at ICON?

To become a Clinical Trial Associate (CTA) at ICON, candidates should have at least two years of experience in a similar role within CRO or pharmaceutical companies. A background in oncology clinical research is preferred. Strong communication skills and a good command of the English language are essential to effectively collaborate with various teams and monitor trial progress.

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How does ICON promote diversity and inclusion in the workplace for CTAs?

ICON is deeply committed to diversity and inclusion in the workplace. We believe that a diverse workforce leads to greater innovation and success. Our culture prioritizes inclusivity, providing an environment where every Clinical Trial Associate (CTA) can thrive regardless of background, and we actively encourage applicants from underrepresented groups to apply.

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Common Interview Questions for CTA
Why do you want to work as a Clinical Trial Associate (CTA) at ICON?

Express your enthusiasm for the position and the values of ICON as an organization. Discuss how the role aligns with your career goals, your passion for clinical research, and your desire to contribute to impactful studies that improve patient outcomes.

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EMPLOYMENT TYPE
Full-time, remote
DATE POSTED
April 12, 2025

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