Hybrid Clinical Trials Job at IQVIA South Korea
Are you looking for a Clinical Trials Assistant job where you can build a career in clinical research and support global clinical trials? The Clinical Trials Assistant Job role at IQVIA in Korea offers an exciting opportunity to work closely with Clinical Research Associates and regulatory teams to manage essential clinical documentation and trial operations. Based in Seoul, this Hybrid Clinical Trials Job at IQVIA Careers is ideal for candidates seeking hands-on experience in Trial Master File (TMF) management, clinical data coordination, and regulatory compliance, while contributing to the development of innovative medical treatments.
About the Company:
IQVIA is a global leader in clinical research services, healthcare analytics, and commercial insights. The company connects data, technology, and expertise to accelerate the development and commercialization of medical treatments. With a strong global presence, IQVIA supports pharmaceutical, biotechnology, and healthcare organizations in improving patient outcomes and advancing population health worldwide.
Job Details:
- Job Role: Clinical Trials Assistant (Sponsor Dedicated)
- Location: Seoul
- Job Type: Full-Time
- Work Mode: Hybrid
- Job ID: R1535408
Key Responsibilities:
- Assist CRAs and regulatory teams in maintaining and updating the Trial Master File (TMF) in this Clinical Trial Job in Korea
- Support preparation, handling, distribution, and archiving of clinical documents
- Review study files periodically for completeness and compliance
- Manage clinical trial supplies and track documentation such as CRFs and queries as a Clinical Trial Assistant
- Act as a central communication point for the clinical team at IQVIA Careers
- Support clinical data flow and documentation tracking systems
- Assist in site visits and clinical monitoring activities (after training) in this Clinical Trial Job in Korea
- Ensure all processes follow SOPs and regulatory guidelines
Educational Requirements for this Job:
- Bachelor’s degree in Life Sciences, or related field
- An equivalent combination of education and experience may be considered
- Minimum 1 year of clinical research or CTA-related experience preferred
Skills Required:
- Knowledge of clinical research processes and documentation
- Understanding of GCP and ICH guidelines
- Strong organizational and time management skills
- Proficiency in MS Word, Excel, and PowerPoint
- Good written and verbal communication skills (English proficiency required)
- Ability to work collaboratively with teams and stakeholders
- Attention to detail and accuracy in documentation
Benefits of the Clinical Trial Job:
- Opportunity to work in a global clinical research organization
- Hybrid work flexibility
- Exposure to international clinical trials and regulatory processes
- Career growth in clinical research and trial management
- Collaborative and professional work environment
- Contribution to the development of innovative healthcare treatments
