This is a fully remote position, open to applicants in Arizona, +5 more states.

📋 Description

• Conduct site qualifications, initiation, monitoring, and closure 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 efficient study execution.

• Review data and resolve queries to ensure the production of high-quality clinical data.

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

• Operate within a sponsor-dedicated model, leveraging ICON’s global expertise.

⛳️ Requirements

• Bachelor’s degree in a scientific or healthcare-related discipline.

• At least 2 years of experience as a Clinical Research Associate.

• Experience in oncology monitoring is mandatory.

• 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 as part of a team in a dynamic environment.

• Willingness to travel up to 50% within their region (West, Central, or South) as necessary.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where 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 advancement pathways.