Louisiana Licensed Clinical Research Associate

Job Summary

A company is looking for a Clinical Research Associate to monitor and participate in clinical trials remotely.

Key Responsibilities

• Conduct site monitoring visits to ensure compliance with GCP, ICH, and regulatory guidelines
• Support subject recruitment and adapt recruitment plans as needed
• Maintain accurate site documentation, including visit reports and regulatory files

Qualifications

• At least 2 years of onsite oncology monitoring experience
• Proficiency in CTMS, EDC, and Microsoft Office Suite
• Strong knowledge of GCP, ICH guidelines, and regulatory requirements
• Experience in site management, patient recruitment, and clinical trial documentation
• Bachelor's degree in life sciences, nursing, or a related field (advanced degree preferred)