About this role
Study Coordinator at unc. Location: Chapel Hill, North Carolina, United States. Role: recruiting participants, documenting visits, coordinating visits Requirements: Bachelor's degree plus 1 year related experience or equivalent; experience coordinating oncology clinical trials; knowledge of ICH/GCP and federal regs; SOCRA or ACRP preferred; strong documentation, communication, and computer skills; occasional evenings/weekends. Category: Research and Development (R&D) Seniority: Entry Level Certifications: socra, acrp Commitment: Full Time Workplace: Onsite Languages: English