Clinical Research Associate – All Level

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

📋 Description

• Carry out site qualification, initiation, monitoring, and closure visits for clinical trials.

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

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

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

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

• Assume responsibility for monitoring deliverables in clinical trials and work in a collaborative manner.

⛳️ 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, relevant regulations, and ICH-GCP guidelines.

• Excellent organizational and communication skills, with a keen attention to detail.

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

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

• Legal eligibility 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 schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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