Clinical Trial Manager

Description:

We are continuing to expand our CTM Team within a client dedicated FSP role. This role requires you to Lead and Manage trials and teams across a cluster, so you will be working with teams in the UK, ROI, Belgium and The Netherlands. You will be involved in Oncology studies, or CAR-T trials, and/or Haematology, Immunology and Cardiovascular diseases.

Other Key duties include:
 

• Reviewing Protocols and Consent forms
• Organising Kick off meetings
• Training CRA teams
• Organising INV meetings
• Monitoring and tracking start up activities
• Co-ordinating the submission process and ethics approvals
• Supporting monitoring teams – the CRAs will approach the CTM for advice when needed
• Oversee the monitoring activities e.g. review trip reports, check compliance, co-monitoring
• Developing the strategy, tools and training to oversee and assess the performance of CRA’s – trip report review, monitoring tool compliance, AFV
• Identifying risks, follow up on issues, timely response to audit inspection reports