Clinical Trials Associate

This is a fully remote position, open to applicants in South Korea.

📋 Description

• Provide administrative support and project tracking to the clinical project team.

• Ensure that all tasks for assigned projects are executed promptly and accurately.

• Organize and monitor system access for project team members.

• Maintain and conduct quality audits on project documentation.

• Assist the project team in preparing and shipping clinical trial documentation.

• Oversee version control and quality assurance of project documentation.

• Submit documents to the trial master file.

• Track and maintain information pertinent to the project.

• Generate and distribute minutes from project-related meetings.

• Keep current records of participating site and personnel information.

• Organize and oversee the distribution of project-specific training for the project team.

• Perform additional duties as assigned.

⛳️ Requirements

• Degree-level qualification or equivalent experience, along with a minimum of one year in a related role.

• Exceptional written and verbal English skills, as well as fluency in the local language.

• Strong interpersonal abilities.

• Capability to work both independently and collaboratively as part of a team.

• A sense of urgency and the ability to adapt in a fast-paced and dynamic environment.

• Proficient in managing multiple tasks while exercising independent judgment.

• Strong attention to detail and a commitment to quality of work.

• Excellent organizational and problem-solving skills.

• Proficient in MS Office applications, including Outlook, Word, Excel, and PowerPoint.

• Knowledge of ICH, GCP, and FDA or EU directive regulations (as applicable).

🏝️ Benefits

• Opportunities for global team events.

• A diverse and inclusive work environment.

• Professional development opportunities.