in line with GCP requirements.

Key Responsibilities

• Coordinate clinical trials from start-up through to close-out
• Manage participant recruitment, screening, study visits and follow-up
• Conduct protocol-required assessments and clinical procedures
• Maintain study documentation, source data and EDC systems
• Ensure compliance with ICH-GCP, ethics and regulatory requirements
• Support monitoring visits, audits and sponsor interactions
• Collaborate with internal and external stakeholders
• Contribute to quality improvement initiatives and site performance

About You

• 2+ years' experience as a Senior, Lead or experienced Clinical Research Coordinator
• Strong knowledge of clinical trial operations and ICH-GCP
• Experience within commercially sponsored clinical trials
• Excellent organisational and stakeholder management skills
• Ability to manage multiple studies in a fast-paced environment
• Passion for participant care and research excellence
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