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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