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

📋 Description

• Perform site qualification, initiation, monitoring, and close-out visits for clinical trials.

• Ensure adherence to protocols, maintain data integrity, and prioritize patient safety throughout the trial lifecycle.

• Collaborate with investigators and site personnel to ensure seamless study execution.

• Conduct data review and address queries to uphold high standards of clinical data quality.

• Assist in the preparation and evaluation of study documentation, including protocols and clinical study reports.

• Assume accountability for clinical trial monitoring deliverables and engage in collaborative efforts.

⛳️ Requirements

• A Bachelor's degree in a scientific or healthcare-related discipline.

• At least 2 years of experience as a Clinical Research Associate.

• Comprehensive understanding of clinical trial processes, regulatory requirements, and ICH-GCP guidelines.

• Excellent organizational and communication abilities, with a strong attention to detail.

• Capability to work both independently and collaboratively in a dynamic environment.

• Willingness to travel as necessary (approximately 60%).

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

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