Clinical Research Coordinator - Remote

Overview

The Clinical Research Coordinator plans, coordinates, and manages activities related to clinical trials, ensuring compliance with regulatory bodies and patient safety.

In Short

• Plan and manage clinical trial activities.
• Interface with clinical staff to identify eligible patients.
• Provide education to hospital personnel and patients.
• Collect and maintain clinical data and regulatory documents.
• Ensure compliance with study protocols and regulatory agencies.
• Monitor patients as per study requirements.
• Maintain good clinical practices.
• Perform other duties as assigned.
• Adhere to ethical and legal standards.
• Comply with data security guidelines.

Requirements

• Minimum Associate's degree or equivalent experience.
• 1-3 years of related experience preferred.
• Bachelor’s Degree is preferred.
• Research-related certification (e.g., CCRC, ACRP-CP, CCRP) is preferred.
• Driver's license may be required.

Benefits

• Work for a leading health organization.
• Access to a wide range of health-related services.
• Opportunities for professional growth and development.
• Comprehensive benefits package.
• Supportive work environment.