Senior Clinical Research Associate

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

📋 Description

• Provides comprehensive support to clinical project teams and study sites involved in clinical research studies.

• Complies with relevant protocols, standard operating procedures (SOPs), and all applicable guidelines and regulatory standards (e.g., ICH-GCP, GPP).

• Serves as the primary point of contact for study sites.

• Manages all aspects of study site operations to ensure the protection of patient safety.

• Evaluates factors that could impact the safety of subjects/patients and the integrity of clinical data.

• Independently performs all types of site visits, including initiation, routine monitoring, and close-out visits.

• Cultivates and maintains positive working relationships with investigators and study personnel.

⛳️ Requirements

• Bachelor's degree or international equivalent, or a comparable combination of education and experience, preferably in a business, scientific, or healthcare field.

• At least 2 years of on-site monitoring experience; 1 year of oncology experience is preferred.

• Strong proficiency in the Microsoft Office suite (Outlook, Word, Excel, and PowerPoint).

• Customer service-oriented attitude; demonstrates adaptability and teamwork.

• Ability to maintain attention to detail over prolonged periods, ensuring high accuracy.

• Fluent in English, with strong verbal and written communication skills.

• Familiarity with the drug development process.

🏝️ Benefits

• Health insurance

• Flexible work arrangements

• Professional development