Clinical Trials Assistant (Clinical Research)

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

• Support Clinical Research Associates and Regulatory and Start-Up teams in maintaining accurate clinical documents and systems, including Trial Master Files.
• Prepare, handle, distribute, file, and archive clinical documentation and reports in line with procedures and project scope.
• Review study files for completeness and track site compliance and performance within project timelines.
• Coordinate clinical trial supplies, Case Report Forms, queries, and clinical data flow.
• Act as a central contact for project communications, correspondence, and related documentation.
• Assist with clinical monitoring duties during site visits after completing required training.

Requirements

• At least 1 year of experience in a Clinical Trials Assistant role.
• Strong spoken and written English communication skills are required.
• Working knowledge of Microsoft Word, Excel, and PowerPoint.
• Effective time management, organizational, communication, and relationship-building skills.
• Basic knowledge of Good Clinical Practice and International Conference on Harmonization guidelines.
• Knowledge of applicable clinical trial protocol requirements after company training.

Culture & Benefits

• Full-time employment supporting global clinical research programs.
• Work alongside Clinical Research Associates, Regulatory and Start-Up specialists, managers, coworkers, and clients.
• Training is provided for applicable regulatory and protocol requirements.
• Integrity and truthful, complete application information are required throughout the hiring process.