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

📋 Description

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

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

• Partner with investigators and site personnel to support 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, such as protocols and clinical study reports.

• Design and evaluate clinical trials, interpret intricate medical data, and aid in the progression of innovative treatments and therapies.

⛳️ 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 attention to detail.

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

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

• Employment with ICON is contingent upon possessing the legal right 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.