Senior Clinical Research Associate

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

📋 Description

• Conduct 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 process.

• Work in partnership with investigators and site personnel to ensure efficient study execution.

• Engage in data review and resolve queries to uphold the quality of 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.

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

• Comprehensive understanding of clinical trial procedures, regulations, and ICH-GCP guidelines.

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

• Capability to work both independently and as part of a team in a fast-paced environment.

• Willingness to travel a minimum of 60% of the time (both internationally and domestically - via air and ground) and must possess a valid driver’s license.

• Employment with ICON is dependent on having the legal right to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary with performance-related incentives.

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

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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