This is a fully remote position, open to applicants in Arizona, +6 more states.

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

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

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

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

⛳️ Requirements

• A 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 essential.

• Comprehensive understanding of clinical trial processes, regulations, and ICH-GCP guidelines.

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

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

• Willingness to travel as necessary, up to 60-75% within the designated region (Western region preferred or any location).

• Must have 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 insurance and disability coverage.

• Employee assistance programs and wellness resources.

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