Clinical Trials Associate

Worldwide Clinical Trials

. Arrange and track system access for the project team .

Posted 9/15/2026full-timeRemote • South KoreaJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates strong organizational skills and attention to detail in managing project documentation and tracking system access. Proficient in maintaining compliance with ICH, GCP, and FDA or EU regulations while effectively communicating in English and the local language.

Highest-signal resume keywords

Project Documentation ManagementICH, GCP, FDA Regulations KnowledgeMS Office ProficiencyStrong Interpersonal SkillsOrganizational and Problem-Solving Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Project Documentation ManagementQuality ControlClinical Trial DocumentationVersion ControlMeeting Minutes GenerationTask TrackingRegulatory ComplianceDocument Quality AuditingSite Information MaintenanceTraining Distribution

Soft Skills

Excellent Written and Verbal CommunicationStrong Interpersonal SkillsAbility to Work IndependentlyAdaptability in Fast-Paced EnvironmentsAttention to Detail

Tools & Technologies

MS Office ApplicationsOutlookWordExcelPowerPoint

Industry Keywords

Clinical TrialsInvestigator Site FileTrial Master FileProject ManagementRegulatory Compliance

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Arrange and track system access for the project team
Maintain and quality audit documents on project portals
Assist with preparation and shipment of clinical trial documentation, including Investigator Site File
Maintain version and quality control of project documentation and submit to trial master file
Track and maintain project-related information, including site medical question and answer logs
Generate and distribute minutes for project-related meetings, including Sponsor and Internal Management meetings
Maintain current participating site and personnel information
Arrange and track distribution of project-specific training to the project team
Perform other duties as assigned

Requirements

What you’ll need

Excellent written and verbal English
Fluency in the language of the country of location
Strong interpersonal skills
Ability to work independently and as a team member
Sense of urgency and ability to be adaptable in a fast-paced and rapidly changing environment
Ability to handle multiple tasks and exercise independent judgment
Strong attention to detail and focus on quality of work
Strong organizational and problem-solving skills
Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)
Degree level qualification or equivalent experience
Minimum of one years’ experience in a related role
Skill sets and proven performance equivalent to the above

Benefits

Comp & perks

Equal employment opportunities regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law