Clinical Research Coordinator Senior

About this role

Responsibilities

• Oversees the day-to-day implementation of clinical research studies in accordance with Good Clinical Practice (GCP), including participant identification, recruitment, screening, informed consent, and follow-up across clinic-based and remote settings.
• Prepares and submits materials to the Institutional Review Board (IRB) and other regulatory bodies, maintaining compliance with protocol requirements and applicable regulations in a timely manner.
• Develops and maintains systems for study tracking, including participant status, recruitment progress, study milestones, and required documentation.
• Implements and oversees data collection and management processes, including electronic data capture systems, to ensure data quality, integrity, and adherence to protocol and GCP standards.
• Conducts ongoing quality assurance activities, including review of study procedures and documentation, to ensure accurate data capture and protocol compliance. Prepares for and supports monitoring visits and audits.