Clinical Research Associate Jobs – Fortrea, a leading global contract research organization (CRO), is hiring a Clinical Research Associate II in Seoul, South Korea.
This hybrid, full-time role is ideal for experienced monitors with at least 1.5 years of independent monitoring experience who are fluent in Korean and proficient in English.
Join a dynamic team managing clinical trials, ensuring regulatory compliance, and driving study success in a collaborative, growth-oriented environment.
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About the Company
Fortrea is a global leader in clinical research and drug development services, formed through the spin-off of Covance’s clinical business. The company partners with pharmaceutical, biotechnology, and medical device sponsors to accelerate clinical trials, ensure regulatory compliance, and deliver high-quality data.
With a strong presence across Asia-Pacific, including South Korea, Fortrea emphasizes scientific excellence, operational efficiency, patient safety, and a supportive culture that fosters career development and innovation in clinical research.
Job Details
- Company Name: Fortrea
- Position: Clinical Research Associate II (CRA II)
- Experience: Minimum 1.5 years of independent monitoring experience
- Qualification: Relevant degree in life sciences, pharmacy, nursing, or related field (specific degree not listed; clinical research background required)
- Location: Seoul, South Korea
- Work Type: Full-time, Hybrid
- Job ID: 255394
Job Description
As a Clinical Research Associate II, you will play a key role in managing and monitoring clinical trials, ensuring compliance with protocols, ICH-GCP, and local regulatory requirements.
You will also support site selection, initiation, close-out activities, and mentor junior CRAs while collaborating with cross-functional teams to meet study timelines and quality standards.
Clinical Research Associate II (CRA II)
- Department: Clinical Operations
- Market: Clinical Research Services – Pharmaceuticals & Biotech
- Role: Clinical Research Associate II
- Experience: Minimum 1.5 years of independent monitoring experience
- Education/Qualification: Degree in life sciences, pharmacy, nursing, or related field
Skills/Qualifications
- Minimum 1.5 years of independent clinical trial monitoring experience
- Strong knowledge of ICH-GCP guidelines and local South Korean regulatory requirements
- Excellent communication, organizational, and problem-solving skills
- Fluency in Korean and professional proficiency in English (both written and spoken)
- Ability to work independently and as part of a cross-functional team
- Willingness to travel for site monitoring visits as required
Key Responsibilities
- Conduct site monitoring visits (selection, initiation, routine monitoring, and close-out)
- Ensure adherence to study protocols, ICH-GCP, and applicable regulatory guidelines
- Support site selection, initiation, and close-out activities
- Collaborate with cross-functional teams to maintain study timelines and quality standards
- Provide mentorship and guidance to junior CRAs when needed
- Maintain accurate documentation and timely reporting of monitoring activities
- Identify and resolve site-level issues to ensure study integrity and compliance
Benefits/Perks
- Career growth in a global CRO with strong presence in Asia-Pacific
- Hybrid working model with flexibility
- Exposure to diverse clinical trials and therapeutic areas
- Professional development and mentorship opportunities
- Competitive compensation and comprehensive benefits
- Inclusive, collaborative work culture focused on innovation and patient impact
How to Apply
Apply directly through the Fortrea careers portal: https://careers.fortrea.com (search for Job ID 255394 or “Clinical Research Associate II Seoul”).
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Fortrea Career page.
Submit your updated resume highlighting monitoring experience, regulatory knowledge, and language proficiency (Korean & English). For more CRA jobs, clinical research associate openings, pharma clinical roles, and careers in South Korea, visit Pharma Recruiter.
Apply now and advance your clinical monitoring career with Fortrea in Seoul!
Why You Should Join
Fortrea offers a dynamic, hybrid working environment where experienced CRAs can take ownership of monitoring activities while mentoring juniors and contributing to global clinical trials.
With a strong focus on regulatory compliance, scientific excellence, and career development, the company provides meaningful work, professional growth, and the opportunity to make a real impact on drug development and patient outcomes.
Joining Fortrea means working in a collaborative, innovative organization that values expertise, diversity, and excellence in clinical research.
FAQs
What is the minimum monitoring experience required for the CRA II role?
Minimum 1.5 years of independent monitoring experience is required.
Is Korean language fluency mandatory?
Yes—fluency in Korean and proficiency in English are essential for this Seoul-based role.
What is the work arrangement?
Full-time, hybrid model (combination of office and remote work).
How do I apply for this Clinical Research Associate position?
Apply directly on the Fortrea careers portal using Job ID 255394 and submit your resume with relevant monitoring and regulatory experience clearly highlighted.
