| Aris project managers possess an average of 14 years clinical research experience. Their expertise spans a variety of therapeutic areas and the practical logistics of trial management. With backgrounds and extensive work experience in pharma and biotech companies, as well as large CROs, our project managers are well versed in study and case report form (CRF) design, effective monitoring practices, and site and personnel management.
Our managers coordinate all aspects of the trial process, including budget development, creating and managing timelines, writing regular status reports and enabling communications between the client and team members. They manage other study vendors, such as central labs, central institutional review boards (IRBs), and data management groups — all of the vital components that contribute to the success of a clinical trial. This single point of contact model saves time, reduces cost, and streamlines the decision making process.
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