About this role
Clinical Study Specialist at Regeneron. Location: Armonk or Warren. Role: organizing reports, tracking enrollment, coordinating meetings Requirements: Bachelor's degree with 2+ years clinical industry experience; familiarity with trial management systems, IVRS/IWRS, EDC, TMF; Microsoft Project/PowerPoint/Word/Excel; awareness of ICH/GCP; strong organization and communication. Category: Research and Development (R&D) Seniority: Entry Level Tools: Microsoft Project, Microsoft PowerPoint, Microsoft Word, Microsoft Excel, IVRS/IWRS, EDC, TMF Commitment: Full Time Workplace: Hybrid Languages: English