Clinical Trials Associate

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

📋 Description

• Coordinate and monitor system access for members of the project team

• Oversee and conduct quality audits of current document revisions on project portals

• Assist in the preparation and distribution of clinical trial documentation, including the Investigator Site File

• Ensure version control and quality management of project documentation before submission to the trial master file

• Track and uphold project-related information, including logs for medical questions and answers from sites

• Generate and disseminate minutes from project meetings, including those with Sponsors and Internal Management

• Keep up-to-date records of participating site and personnel information

• Organize and monitor the distribution of project-specific training to the team

• Carry out additional assigned responsibilities

⛳️ Requirements

• Degree-level qualification or equivalent experience

• At least one year of experience in a similar role

• Skill sets and proven performance that meet the stated requirements

• Exceptional written and verbal communication skills in English

• Proficiency in the language of the country of location

• Strong interpersonal abilities

• Capability to work independently as well as collaboratively within a team

• Flexibility to adapt to a fast-paced and rapidly evolving environment

• Ability to manage multiple tasks and make independent decisions

• Keen attention to detail and a commitment to quality

• Excellent organizational and problem-solving capabilities

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

• Understanding of ICH, GCP, and FDA or EU directive regulations, as relevant

🏝️ Benefits

• Equal employment opportunities irrespective of protected characteristics

• A diverse and inclusive workplace

• Supportive and cooperative teams

• Accessible leadership

• Opportunities for employees to succeed and thrive