About this role
Clinical Research Coordinator Associate at Stanford University. Location: Stanford, California, United States. Role: managing protocols, recruiting participants, collecting data Requirements: Manage clinical research protocols, prepare regulatory/IRB submissions, recruit and consent participants, collect/process specimens and data, maintain drug accountability, and ensure regulatory compliance. Category: Research and Development (R&D) Seniority: Entry Level Tools: Microsoft Office Certifications: socra, acrp Commitment: Full Time Workplace: Onsite Languages: English