About this role
Clinical Research Assoc III at undefined. Location: Webster, Texas, United States. Role: Monitor sites, Perform visits, Prepare reports Requirements: Bachelor's in life sciences; 3+ years clinical research monitoring; oncology experience; GCP knowledge; trip report review; TMF reconciliation; on-site monitoring experience (3+ years). Category: Research and Development (R&D) Seniority: Mid Level Tools: Electronic Data Capture (EDC), GCP Certifications: certified clinical research associate (ccra), clinical research coordinator (crc) Commitment: Full Time Workplace: Onsite Languages: English