Clinical Operations Team
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