Senior Clinical Research Associate

Job Summary

A company is looking for a Senior Clinical Research Associate (CRA) to support clinical research activities remotely.

Key Responsibilities

• Perform on-site and remote monitoring visits to ensure compliance with GCP, ICH, and regulatory standards
• Collaborate with investigative sites to enhance enrollment efforts and modify recruitment strategies as needed
• Deliver protocol-related training and act as a liaison between study teams and site staff

Required Qualifications

• Minimum of 3 years of recent on-site monitoring experience, including oncology trials
• Experience supporting studies across multiple therapeutic areas, including general medicine
• Working knowledge of CTMS, EDC platforms, and Microsoft Office tools
• Strong understanding of GCP, ICH guidelines, and clinical research regulations
• Bachelor's degree in life sciences, nursing, or a related discipline (advanced degree preferred)