cardiabase as a CRO claims that dedicated and experienced project management is a milestone for the success of a clinical trial.
cardiabase team has
extensive experience in clinical trial management. Overall our activity is based on repeat projects and / or projects issued of referrals from our satisfied customers.
The Project Manager (PM) is the primary contact for all the organizations involved in the conduct of the trial. The PM works with all project team members to ensure problem identification, resolution and respect of study timelines.
One of the tasks in Project Management is the
organisation of meetings, which involves the preparation, participation in and reporting of meetings. These can be Steering Committee meetings, sponsor meetings or investigator meetings.
Apart from the Protocol and CRF, all kinds of documents need to be developed not only to comply with research guidelines, rules and regulations but also to ensure the smooth and fast progress of the trial.
Experience and organisation are the keywords in this part of Project Management.
In close collaboration with the sponsor, the
Clinical Project Manager is responsible for the development and maintenance of numerous manuals and critical documents.
We offer a wide range of paper based / web based central management of clinical dossiers management solutions, including the following:
- Database design and building
- Consistency and quality checks
Indeed our strategy is to provide sponsors with a customized approach that optimally meets sponsors needs and budget.
