Risk

• Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices
• Develop and implement tools, procedures, and processes to ensure quality monitoring
• Contribute to the design, implementation, and delivery of processes, programs, and policies
• Manage and direct the work of lower-level professionals or manage processes and programs
• Ensure accurate and timely documentation and reporting of clinical trial data
• Collaborate with cross-functional teams to support clinical trial activities
• Identify and resolve issues related to clinical trial conduct and data integrity
• Provide training and mentorship to junior staff members

Senior CRA – Oncology, Risk Based Monitoring

Risk & Fraud Lead

Director of Governance and Risk

Trading Risk Manager – EU Timezone

Clinical Governance Manager