Icon plc Clinical Research Vacancies – Work from home
Exciting ICON CRA I Oncology Jobs 2026 | Clinical Research Associate Remote
ICON Strategic Solutions is hiring a Clinical Research Associate I (CRA I) for its Oncology Clinical Monitoring team in South Korea. This home-based opportunity is ideal for clinical research professionals with oncology monitoring experience who are looking to advance their careers in global clinical trials, site monitoring, and clinical operations.
Candidates with expertise in ICH-GCP guidelines, clinical trial monitoring, site management, and oncology studies will have the opportunity to work with one of the world’s leading clinical research organizations while supporting innovative cancer research programs.
Company Overview
ICON plc is a global healthcare intelligence and clinical research organization that partners with pharmaceutical, biotechnology, and medical device companies to accelerate the development of life-changing therapies.
Through ICON Strategic Solutions (FSP), the company provides dedicated clinical research professionals who support clinical development programs worldwide. ICON is recognized for its strong focus on innovation, patient safety, regulatory compliance, and clinical excellence.
Job Role & Responsibilities
As a Clinical Research Associate I, you will support clinical trial monitoring activities and ensure studies are conducted according to protocol requirements, Good Clinical Practice (GCP), and applicable regulations.
Key Responsibilities
Clinical Trial Monitoring
- Coordinate study start-up and monitoring activities.
- Conduct routine site monitoring visits.
- Review study documentation and site records.
- Ensure compliance with study protocols and regulatory requirements.
- Monitor clinical trial progress and site performance.
Site Management
- Develop relationships with investigators and site personnel.
- Provide support to clinical trial sites.
- Address site queries and operational challenges.
- Ensure accurate and timely study documentation.
Clinical Operations
- Complete study status reports and monitoring reports.
- Execute sponsor-generated queries efficiently.
- Support feasibility assessments for new studies.
- Participate in study documentation review activities.
Patient Safety & Compliance
- Ensure patient safety throughout study conduct.
- Verify compliance with ICH-GCP guidelines.
- Maintain regulatory and protocol adherence.
- Identify and escalate study risks when required.
Eligibility / Qualifications
Educational Qualification
Candidates must possess:
- Bachelor’s Degree in Life Sciences
- Pharmacy
- Medicine
- Nursing
- Biotechnology
- Biochemistry
- Microbiology
- Clinical Research
- Or equivalent scientific qualification
Eligible Courses
B.Pharm, M.Pharm, Pharm.D, MBBS, BDS, B.Sc Life Sciences, M.Sc Life Sciences, Biotechnology, Biochemistry, Microbiology, Nursing, Clinical Research, Medical Sciences, Healthcare Sciences.
Experience Required
Mandatory Requirement
- Prior Oncology Clinical Trial Experience
- Clinical Trial Monitoring Experience
Candidates with experience in:
- Site Monitoring
- Oncology Clinical Trials
- Clinical Research Associate (CRA) Activities
- Clinical Operations
- Site Management
- Regulatory Compliance
will be preferred.
Required Skills
Clinical Research Skills
- Clinical Trial Monitoring
- Site Management
- Oncology Research
- Clinical Operations
- Trial Documentation
- Feasibility Assessment
- Monitoring Visit Management
- Investigator Site Coordination
Regulatory Knowledge
- ICH-GCP Guidelines
- Clinical Trial Regulations
- Patient Safety Compliance
- Regulatory Documentation
Professional Skills
- Communication Skills
- Stakeholder Management
- Problem Solving
- Time Management
- Organizational Skills
- Medical Data Review
Location & Salary
Location: Seoul, South Korea (Home-Based/Remote)
Travel Requirement: Approximately 60%
Approximate Salary: ₩55 Million – ₩85 Million per year (Estimated industry range based on CRA I oncology positions in South Korea)
Why Join ICON?
- Work with a globally recognized CRO.
- Exposure to international oncology clinical trials.
- Home-based working model.
- Career advancement in clinical research and monitoring.
- Opportunities to work with leading pharmaceutical sponsors.
- Strong focus on employee development and professional growth.
Application Process
Interested candidates can apply through the official ICON careers portal:
https://careers.iconplc.com/job/clinical-research-associate-i-in-korea-seoul-jid-51377
Candidates should ensure their resume highlights oncology monitoring experience, clinical trial exposure, site management expertise, and GCP knowledge.
Frequently Asked Questions (FAQs)
1. Is oncology experience mandatory?
Yes. Oncology study experience is a mandatory requirement for this position.
2. Is this a remote role?
Yes. The role is home-based in South Korea.
3. How much travel is required?
Approximately 60% travel is expected for monitoring activities.
4. What qualifications are accepted?
Candidates with degrees in Pharmacy, Medicine, Life Sciences, Nursing, Biotechnology, or related scientific disciplines can apply.
5. What regulatory knowledge is required?
Applicants should have strong knowledge of ICH-GCP guidelines and clinical trial regulations.
6. What is the primary responsibility of a CRA I?
The role focuses on clinical trial monitoring, site management, regulatory compliance, and patient safety oversight.
Job Summary
| Category | Details |
|---|---|
| Company | ICON Strategic Solutions |
| Department Vacancies | Clinical Research Associate I (CRA I) – Oncology |
| Qualification | B.Pharm, M.Pharm, Pharm.D, MBBS, Nursing, Life Sciences |
| Experience | Clinical Trial Monitoring with Oncology Experience |
| Location | Seoul, South Korea (Home-Based) |
To apply for this job please visit careers.iconplc.com.
