Clinical Research Associate

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

📋 Description

• Engage in a sponsor-dedicated model to support client trials focused on cardiovascular health and obesity.

• Design and evaluate clinical trials, analyze intricate medical data, and contribute to the development of innovative treatments and therapies.

• Carry out site qualification, initiation, monitoring, and closing visits.

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

• Collaborate with investigators and site personnel to ensure the seamless execution of studies.

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

• Assist in the preparation and review of study-related documentation, including protocols and clinical study reports.

⛳️ 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, regulations, and ICH-GCP guidelines.

• Excellent organizational and communication abilities, with a keen eye for detail.

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

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

• Must reside in South, TX.

• Employment with ICON is subject to possessing the legal right to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-based incentives.

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

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellness resources.

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