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

📋 Description

• Perform 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.

• Collaborate with investigators and site personnel to ensure a seamless 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, including protocols and clinical study reports.

• Oversee sponsor-specific cardio and obesity trials.

• Take charge of clinical trial monitoring deliverables and work alongside study teams.

⛳️ 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 skills, with a keen attention to detail.

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

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

• Must reside in South, TX.

• 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 where applicable.

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellness resources.

• Learning and development opportunities through structured training and career pathways.