Clinical Research Associate

Job Summary

A company is looking for a Clinical Research Associate.

Key Responsibilities

• Support site initiation, ongoing management, and close-out activities in accordance with study timelines
• Ensure compliance with study protocol, ICH-GCP, FDA regulations, and company SOPs
• Provide oversight of CRO CRAs and site management activities, and maintain a compliant Trial Master File

Required Qualifications

• Bachelor's degree in life sciences, nursing, or a related field; advanced degree preferred
• Minimum of 3+ years of clinical operations experience in biotech, pharma, or CRO environments
• Prior experience in site management and CRO oversight strongly preferred
• Strong knowledge of ICH-GCP, FDA regulations, and global clinical trial requirements
• Experience with EDC systems, CTMS, eTMF, and safety reporting processes