Senior Clinical Research Associate

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

📋 Description

• Assists in identifying potential investigators

• Oversees the initiation of studies and regulatory compliance

• Guarantees that sites are consistently prepared for inspections

• Manages study materials and drug accountability at the study site

• Conducts monitoring visits and performs Source Data Review

⛳️ Requirements

• Bachelor's degree in a relevant field, ideally in life sciences

• Strong understanding of international guidelines, particularly ICH-GCP

• Fundamental knowledge of GMP/GDP

• Solid medical knowledge and capacity to learn about relevant Client Therapeutic Areas

• Basic comprehension of the drug development process

• Good grasp of Clinical Study Management, which includes monitoring, handling study drugs, and data management

• Willingness to travel domestically and internationally as needed

🏝️ Benefits

• Health insurance

• Flexible working hours