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

📋 Description

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

• Ensure adherence to protocols, data integrity, and patient safety throughout the entire trial process.

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

• Conduct data reviews and address queries to uphold the quality of clinical data.

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

• Assume responsibility for clinical trial monitoring deliverables and foster collaborative efforts.

⛳️ Requirements

• 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, regulations, and ICH-GCP guidelines.

• Excellent organizational and communication abilities, with a keen eye for detail.

• Capacity to work independently and as part of a team in a dynamic environment.

• 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 options.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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

• An inclusive and accessible work environment.

• Reasonable accommodations provided during the recruitment process.