Clinical Trials Associate

Worldwide Clinical Trials

. Arrange and track system access for project team members .

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

Core Competencies

Role fit

Core Competencies

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Demonstrates strong organizational skills and attention to detail in managing project documentation and compliance with ICH, GCP, and FDA regulations. Proficient in maintaining project-related information and facilitating effective communication within project teams.

Highest-signal resume keywords

Project Documentation ManagementICH, GCP, And FDA Regulations KnowledgeExcellent MS Office SkillsStrong Interpersonal SkillsFluency In English

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project Documentation ManagementQuality ControlClinical Trial Documentation PreparationVersion ControlData TrackingMeeting Minutes GenerationTraining Distribution ManagementProblem-SolvingAttention To DetailOrganizational Skills

Soft Skills

Strong Interpersonal SkillsAbility To Work IndependentlyTeam CollaborationAdaptabilityJudgment

Tools & Technologies

MS OfficeOutlookWordExcelPowerPoint

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 project team members
Maintain and quality audit current document revisions 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 it to the 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 project-specific training distribution to the project team
Perform other assigned duties

Requirements

What you’ll need

Degree level qualification or equivalent experience
Minimum of one year of experience in a related role
Skill sets and proven performance equivalent to the stated requirements
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
Ability to adapt 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
Strong organizational and problem-solving skills
Excellent MS Office skills, including Outlook, Word, Excel and PowerPoint
Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations, as applicable

Benefits

Comp & perks

Equal employment opportunities regardless of protected characteristics
Diverse and inclusive work environment
Supportive and collaborative teams
Accessible leadership
Employee opportunities to succeed and thrive