About this role
Clinical Research Quality Control Specialist. at Monroe Biomedical Research. Location: Bangalore, Karnataka, India. Role: conducting reviews, documenting findings, communicating findings Requirements: 3+ years site-level clinical research experience, strong knowledge of ICH-GCP, proficiency with CRIO/CTMS and Microsoft Office, ability to interpret complex protocols and document QC findings. Category: Research and Development (R&D) Seniority: Mid Level Tools: CRIO, CTMS, Microsoft Office Commitment: Full Time Workplace: Remote Languages: English