Rapid identification of potential investigators and their patient populations is the first step in making sure your study’s timeline remains on-track. Our vast internal database and extensive external tools and connections help ensure that no matter the size or location, we have the resources to meet our clients' needs quickly with a skilled, effective team.

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We make sure clients are regularly updated, and that all site communications are documented and accessible for review. The rigorous oversight not only helps us recruit sales and meet enrollment goals, it helps ensure that protocol requirements are satisfied, and that trials are run safely and smoothly.
 

Key activities performed by Clintract:

     o Selecting qualified investigators
     o Training investigators and site staff on protocol requirements, best practices, and technology tools, such as  
        Electronic Data Capture (EDC) and safety systems
     o Implementing participant-retention programs
     o Monitoring for compliance with study plan, protocol, and IRB review
     o Controlling investigational products
     o Reporting safety data
     o Informing sites about performance and contractual issues
     o Serving as a site’s contact for communicating with Clintract, sponsors, and IRBs

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Clintract’s site management staff ensures the integrity of clinical trials by resolving eligibility issues, handling adverse events, monitoring protocol compliance, and dealing with other concerns.

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Clintract has the resources to manage programs of any scale, from a single-center study to a large, multinational study involving multicultural sites with unique needs. Regardless of the project complexity, Clintract applies appropriate technology to meet study requirements and train site personnel in the procedures required to achieve optimal results.