Study Management
Aris study managers possess an average of 15 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 start-up, site selection, 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 (IRB), and data management groups - all of the vital components that contribute to the success of a clinical trial. This primary point-of-contact model saves time, reduces cost, and streamlines the decision making process.
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 (IRB), and data management groups - all of the vital components that contribute to the success of a clinical trial. This primary point-of-contact model saves time, reduces cost, and streamlines the decision making process.
Aris Clinical, Inc.
369-B Third Street #231
San Rafael, CA 94901
Located in the Greater San Francisco Bay Area
Email: info@arisclinical.com
Phone: 415.785.1844
369-B Third Street #231
San Rafael, CA 94901
Located in the Greater San Francisco Bay Area
Email: info@arisclinical.com
Phone: 415.785.1844
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