Clinical Research Associate

This is a fully remote position, open to applicants in Florida, +1 more state.

📋 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.

• Collaborate with investigators and site personnel to facilitate the effective execution of studies.

• Perform data reviews and resolve queries to uphold high-quality clinical data standards.

• Assist in the preparation and evaluation of study documentation, including protocols and clinical study reports.

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

• Operate within a sponsor-dedicated model, supporting trials related to cardio and obesity.

⛳️ Requirements

• A bachelor's degree in a scientific or healthcare-related discipline.

• A minimum of 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.

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

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

• Employment with ICON is conditional 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 wellbeing programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

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