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

📋 Description

• Design and analyze clinical trials, interpreting intricate medical data.

• Participate in clinical trial monitoring activities and take ownership of deliverables.

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

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

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

• Conduct data reviews and address queries to ensure high-quality clinical data.

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

⛳️ Requirements

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

• A minimum of 2 years of experience as a Clinical Research Associate.

• Comprehensive knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

• Strong organizational and communication skills, with a keen eye for detail.

• Ability to work both independently and collaboratively in a fast-paced environment.

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

• Employment with ICON is conditional upon having the legal right to work in the country where the role is based.

🏝️ 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.