Clinical Trials Assistant (1 Year Contract)

Location: Seoul, Republic of Korea

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Maintain clinical documents and systems, including the Trial Master File, to track site compliance and performance.
• Prepare, distribute, file, and archive clinical documentation and reports according to procedures and project requirements.
• Review study files for completeness and support Clinical Research Associates and Regulatory and Start-Up teams.
• Prepare and track clinical trial supplies and related documentation.
• Track Case Report Forms, queries, and clinical data flow.
• Coordinate designated project communications and may accompany CRAs on site visits after completing required training.

Requirements

• Preferred: at least 1 year of Clinical Trial Assistant experience within a CRO or pharmaceutical company.
• Working knowledge of Microsoft Word, Excel, and PowerPoint.
• Effective time-management and organizational skills.
• Ability to maintain effective relationships with coworkers, managers, and clients.
• Awareness of Good Clinical Practice and International Conference on Harmonization guidelines, as provided in company training.
• Knowledge of applicable clinical trial protocol requirements, as provided in company training.

Culture & Benefits

• Full-time, one-year contract position.
• Work alongside clinical research and regulatory teams supporting clinical trial delivery.
• Training is provided for applicable regulatory and protocol requirements.