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Clinical Trials Assistant

8-15 years
Not Disclosed
10 June 25, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Clinical Trials Assistant – Seoul, South Korea (Hybrid)

Job Summary:
IQVIA is seeking a Clinical Trials Assistant (CTA) to support ongoing clinical research operations in Seoul, South Korea. This hybrid position is ideal for recent graduates or candidates with prior CTA experience who are looking to grow within a globally recognized healthcare company. The role includes supporting CRAs and regulatory teams with trial documentation, compliance tracking, and communication across clinical projects.


Key Responsibilities:

  • Support Clinical Research Associates (CRAs) and Regulatory & Start-Up (RSU) teams in maintaining accurate clinical documents and Trial Master Files (TMF).

  • Assist with distribution, filing, archiving, and handling of clinical trial documentation per SOPs and project timelines.

  • Perform periodic review of study files for accuracy and completeness.

  • Support clinical supply handling and tracking of Case Report Forms (CRFs), queries, and data flow.

  • Serve as a central communication point for the clinical team on designated projects.

  • May accompany CRAs on-site visits after completing required training.

  • Contribute to administrative tasks and study support activities across trial phases.


Required Skills & Qualifications:

  • Bachelor's degree in life sciences, healthcare, or related field (preferred).

  • Entry-level candidates or those with CTA-related experience are encouraged to apply.

  • Good written and verbal English communication skills required.

  • Familiarity with TMF systems, CRFs, and GCP principles is advantageous.

  • Proficient in MS Office tools (Word, Excel, Outlook).

  • Highly organized with attention to detail and teamwork orientation.


Perks & Benefits:

  • Competitive salary (not specified in job description).

  • Global exposure to multinational clinical trials.

  • Career growth opportunities in clinical operations.

  • Hybrid work model in Seoul.

  • Training and mentorship from industry experts.


Company Overview:

IQVIA is a global leader in clinical research, real-world evidence, and healthcare intelligence. We help life sciences companies innovate and commercialize advanced therapies through data-driven insights and operational excellence. Our work supports better healthcare outcomes globally.


Work Mode: Hybrid – Seoul, South Korea
Experience Level: Entry-level or experienced CTA


Ready to begin your journey in clinical research?
Apply now and build a career with IQVIA, a trusted name in global healthcare advancement.