Locations: Spain, Italy

National travel required: 3-4 site visits per month

 Nexa Life Sciences are collaborating with an international clinical research organisation who are seeking additional monitoring support for clinical studies in both Spain and Italy, with the potential expansion into additional locations over the coming months.

For this position, the client requires independent, on-site monitoring experience with 3-4 site visits per month on average.

Key responsibilities include:

• On-site and remote monitoring activities at both local and national level
• Ensure strong communication channels between site and sponsor
• Collaborate with the local study and project management team
• Support with the preparation of clinical study documentation including EC submissions
• Prepare and present accurate and insightful reporting as required
• Ensure audit and inspection readiness at site level
• Site feasibility support as required
• Support training and mentoring for new site staff as required

 If this opportunity is of interest and you would like to learn more, please apply here and forward your up to date CV to sarah.phillips@nexalifesciences.co.uk