Cardiabase believes that a dedicated and time-tested project management system is critical to the success of a clinical trial. The large number of repeat projects or new clients referred to us by satisfied sponsors attests to the quality of the services provided by our highly experienced team in project management.
The Project Manager (PM) is the primary contact for all parties involved in the conduct of the trial. The PM works with all project team members to monitor study progress, ensure rapid problem identification and resolution and ultimately compliance with study timelines.
One important responsibility of Project Managers is meeting organization, which involves planning preparation, participation in and minuting. The various meetings a Project Manager support include Sponsor, Investigator, Clinical Event Adjudication, Data Safety Monitoring Board and Steering Committee meetings.
In addition to the Protocol and CRF, every clinical trial requires that a large number of documents be developed to ensure the expeditious progress of the study and comply with all applicable regulations and guidelines.
Experience and organizational skills are paramount to the success of Project Management, two attributes the Cardiabase team has consistently demonstrated.
Working 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 solutions for the central management of clinical dossiers, including the following:
Flexibility is a tenet of our business philosophy and we provide sponsors with a customized approach that optimally meets their needs and budget.