Clinical Research Associate I

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

📋 Description

• Providing high-quality clinical trial monitoring services

• Collaborating closely with your team and various stakeholders

• Overseeing all tasks related to the setup and monitoring of a study

• Ensuring accurate completion of study status reports and maintaining documentation

• Efficiently managing sponsor-generated queries and taking ownership of study cost-effectiveness

• Involved in the preparation and assessment of study documentation and feasibility studies for new proposals as needed

• Establishing and nurturing strong, collaborative relationships with key stakeholders, clinical investigators, and site personnel

• Guaranteeing adherence to ICON's procedures, protocols, and regulatory standards to ensure patient safety

⛳️ Requirements

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

• Familiarity with ICH-GCP guidelines and the ability to review and assess medical data

• Exceptional written and spoken communication skills in English

• Strong interpersonal skills allowing you to address queries promptly

• Openness to travel as necessary (approximately 60%)

• Experience in oncology studies is essential

🏝️ Benefits

• Competitive base salary along with performance-related incentives

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

• Retirement and pension plans

• Life insurance and disability coverage

• Employee assistance programs and wellness resources

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