Clinical Research Associate

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

📋 Description

• Provide high-quality oversight of clinical trial monitoring activities.

• Organize all tasks involved in the setup and monitoring of a study.

• Prepare precise study status reports and keep study documentation up to date.

• Efficiently handle sponsor-generated inquiries.

• Take charge of ensuring cost efficiency for the study.

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

• Build and sustain collaborative partnerships with key stakeholders, clinical investigators, and site personnel.

• Ensure the safety of patients and adherence to ICON procedures, protocols, and regulatory standards.

⛳️ Requirements

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

• Relevant experience in clinical trial monitoring.

• Familiarity with ICH-GCP guidelines.

• Proficiency in reviewing and analyzing medical data.

• Strong written and verbal communication skills in English.

• Excellent interpersonal skills to address inquiries promptly.

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

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

🏝️ Benefits

• Competitive base salary along with performance-based 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 professional development through structured training and career pathways.