Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

The operations team is responsible for implementing and managing clinical study activities to support MORU investigators. This includes:

  • Handling regulatory submissions for initial protocols and ongoing correspondence with both central and local ethics committees
  • Development of study procedures and documentation and systems necessary to initiate and run studies
  • Conduct of study-specific and general GCP training
  • On-site and remote monitoring of clinical studies to ensure compliance
  • Provide project management services to investigators, including tracking milestones and document management