Managing a clinical trial project requires handling many responsibilities including
- Understanding the key position that randomised controlled trials play in translation research.
- Being able to classify a clinical research study appropriately and have an understanding of the associated regulatory framework.
- Being able to develop a detailed trial protocol compliant with all applicable regulations.
- Understanding the lifecycle of a clinical trial including development of detailed project plans, understanding the approvals process, the importance of a statistical analysis plan, data management plan and risk based trial monitoring
In Medicor Lab we provide you with the information, requirements, techniques, tips and inside knowledge needed to effectively coordinate and manage trials at an investigational site and to take a trial from ethics submission to managing multi-centred studies for a range of clinical trials.