Nexa life Sciences are pleased to be partnering with a global pharmaceutical company who are seeking a clinical expert within study feasibility and initiation activities.  Within this role you will be overseeing a number of studies from feasibility to initiation, including supporting with subsequent project deliverables as well as patient recruitment and retention strategy.

This role will be to work within their Oncology portfolio and therefore experience in this field is preferred, as well as experience in early-phase clinical research.

­Key responsibilities will include:

• Site feasibility assessment and subsequent site selection
• Ensure the site is prepared for study initiation including study supplies
• Study start-up activities
• Ensure site staff are full trained with GCP and study protocols
• Site level recruitment strategy and contingency planning
• Collaborate closely with the study team and attend investigator meetings as required
• Oversee the set-up of the CTMA (Clinical Trial Management system) and TMF (Trial Master File)
• Full knowledge of clinical regulations and direct experience on both UK and EU based studies is 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.