GBS C&H CLINICAL RESEARCH OPERATIONS SUPPORT
Core
Support clinical research operations by managing study documents and facilitating Institutional Review Board (IRB) submissions.
Role type
Clinical Research Operations Support
Builds
Clinical trial documentation and regulatory submissions
Domain
Healthcare / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Study document management, IRB submission coordination, protocol development support, SOP creation and maintenance, regulatory compliance, data quality assurance
Preferred skills
Project management, multi-project coordination
Technologies
MS Office
Responsibilities
Assist in study document development and preparation, collaborate with Clinical Research Coordinators and Principal Investigators, manage study status including SAE reporting and study closure, support client interactions during study preparation, assist in protocol and procedure reviews, ensure compliance with GCP and company SOPs
Seniority
Junior, hands-on IC
