Associate Clinical Trial Manager

Job Summary

Supporting the implementation and conduct of clinical research projects, the full-time Associate Clinical Trial Manager will manage large global oncology clinical trials, assist in vendor management, and maintain Trial Master File documents, with options for remote work.

Key responsibilities

• Manage or assist in managing large global oncology clinical trials, ensuring compliance with protocols and regulatory requirements
• Track study progress, maintain status updates, and provide progress reports to project teams
• Maintain and support the eTMF and CTMS platforms, ensuring quality and compliance with relevant guidelines

Required qualifications

• Undergraduate degree in Biological Sciences or related fields with 1-2 years of relevant clinical operations experience
• Experience in trial set-up, monitoring, and close-out of Phases 1-3 clinical trials
• 1-2 years of experience in TMF/document management or clinical trial support
• Familiarity with eTMF systems and Clinical Trial Master Systems
• Practical knowledge of ICH-GCP guidelines and US and ex-US regulations