This is a fully remote position, open to applicants in Kansas, +2 more states.

📋 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 effectively with investigators and site personnel to ensure seamless study execution.

• Perform thorough data reviews 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.

• Design and analyze clinical trials, interpret complex medical data, and support the advancement of innovative treatments and therapies.

• Assume responsibility for clinical trial monitoring deliverables while working in a cooperative manner.

⛳️ 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 skills, with a strong attention to detail.

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

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

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