The project management functional area supports researchers with funding proposals and the acquisition of external funding for clinical trials that adhere to all legal regulations (AMG, MPG, BOń) in phases I to IV and advises researchers in all aspects of clinical research.
The CTC-A can work as a central project office in multi-centric trials.
The project manager helps to realize research work by assuming all of the administrative support, the interface management, and the operative coordination of individual project phases till close out.
The focuses include integration of a project with regards to the administrative demands, the creation and administration of documents for the trial, getting the approval of all of the ethics committees and authorities, supervision and observance of deadlines and durations, the implementation of amendments, and the direction of internal/external correspondence with project partners, external parties, and regulatory contacts.
The goals of project management are:
- efficient and cost-saving project processes
- introduction/adherence of high quality standard
- implementatin of all ethical-legal regulations