Clinical Project Management
The Clinical Project Manager (CPM) assists in the planning and execution of clinical trials while adhering to budget, scope and timelines. The CPM is responsible for managing all aspects of a clinical trial or multiple clinical trials, vendor, CRO, and sites. The CPM provides oversight to ensure that Good Clinical Practice (GCP) and ICH Guidelines are being followed. CPM provides oversight on protocol, patient safety, and data integrity. The CPM will lead planning and communicate with cross-functional study teams to ensure proper execution and conduct of the trial, and will serve as primary contact and resource.
Clinical Research Associates (CRAs) are the foundation for successful delivery of your trial. CRAs are dedicated to the integrity of your study data and patient safety. CRAs work with the investigator site, and team assigned to the clinical trial. CRAs have the experience and skill level to deliver clinical trials within a range of therapeutic areas. CRAs ensure that data is being monitored onsite and remote. The CRAs have experience with Electronic Data Capture (EDC). Our CRAs demonstrate a high level of knowledge with Good Clinical Practice (GCP), and ICH Guidelines are being met.