Clinical Research Associate

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

📋 Description

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

• Guarantee protocol adherence, data integrity, and patient safety throughout the trial duration.

• Work alongside investigators and site personnel to ensure efficient study execution.

• Conduct data reviews and resolve 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 assess clinical trials, analyze intricate medical data, and aid in the development of groundbreaking 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 eye for detail.

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

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

• Employment with ICON is contingent upon possessing the legal right to work in the country where the position is based.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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