Clinical Research Associate

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

📋 Description

• Oversee the organization and monitoring of clinical studies.

• Prepare precise study status reports and maintain comprehensive study documentation.

• Efficiently address sponsor-generated queries and ensure cost-effectiveness of the study.

• Take part in the preparation and evaluation of study documentation and feasibility studies for new proposals.

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

• Safeguard patient safety by adhering to ICON procedures, protocols, and regulatory requirements.

⛳️ Requirements

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

• Relevant experience in clinical trial monitoring.

• Familiarity with ICH-GCP guidelines.

• Capability to review and assess medical data.

• Exceptional written and verbal communication skills in English.

• Strong interpersonal skills to address queries promptly.

• Openness to travel as required, approximately 60% of the time.

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

🏝️ Benefits

• Competitive base salary.

• Performance-based incentives.

• 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 pathways.