About this role
TI Sr Clinical Research Assistant at Department Overview. Location: Portland, Oregon, United States. Role: coordinating trials, submitting regulations, managing data Requirements: Coordinate complex interventional clinical trials, perform regulatory submissions, handle specimen collection and data entry; requires clinical research experience, IRB submission experience, clinical skills (phlebotomy, ECG, vitals), and strong communication. Category: Research Seniority: Entry Level Tools: Epic, OnCore Certifications: citi, ccrp Commitment: Full Time Workplace: Hybrid Languages: English