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

📋 Description

• Execute clinical trial monitoring tasks to an exceptional standard

• Independently and proactively coordinate all activities necessary for setting up and overseeing a study

• Accurately complete study status reports and maintain comprehensive study documentation

• Efficiently manage sponsor-generated inquiries

• Assume responsibility for the financial efficiency of the study

• Contribute to the preparation and evaluation of study documents and feasibility studies for new proposals as needed

• Foster and maintain collaborative relationships with key stakeholders, clinical investigators, and site personnel

• Ensure patient safety by adhering to ICON's procedures, protocols, and regulatory standards

⛳️ Requirements

• Bachelor's degree in medicine, science, or a related field

• Understanding of ICH-GCP guidelines

• Ability to review and assess medical data effectively

• Excellent written and verbal communication skills in English

• Strong interpersonal skills to address inquiries promptly

• Willingness to travel as needed (approximately 60%)

• Relevant experience in clinical trial monitoring

• Legal authorization to work in the country where the position is located

🏝️ Benefits

• Competitive base salary along with performance-related incentives

• Health and wellness programs including medical, dental, and vision coverage where applicable

• Retirement and pension schemes

• Life insurance and disability coverage

• Employee assistance programs and wellness resources

• Opportunities for learning and development through structured training and career advancement pathways