Clinical Research Associate 1

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

📋 Description

• Oversee all processes involved in establishing and monitoring a study.

• Ensure accurate completion of study status reports and maintain all related documentation.

• Efficiently address sponsor-generated queries and take charge of study cost management.

• Engage in the preparation and evaluation of study documentation and feasibility assessments for new proposals as needed.

• Build and sustain cooperative relationships with essential stakeholders, clinical investigators, and site personnel.

• Safeguard patient safety and ensure adherence to ICON procedures, protocols, and regulatory standards.

⛳️ Requirements

• Bachelor's degree in medicine, science, or a related field.

• Familiarity with ICH-GCP guidelines.

• Proficiency in reviewing and assessing medical data.

• Exceptional written and verbal communication skills in English.

• Strong interpersonal skills for timely query resolution.

• Availability to travel as necessary, approximately 60% of the time.

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

• Relevant experience in clinical trial monitoring.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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