Investigator Recruitment and Site Management

Quality trial execution. On time.

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.

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 PharmaNet/i3 include:

• Selecting qualified investigators
• Training investigators and site staff on protocol requirements, best practices, and technology tools, such as Electronic Data Capture (EDC) and safety systems
• Implementing participant-retention programs
• Monitoring for compliance with study plan, protocol, and IRB review
• Controlling investigational products
• Reporting safety data
• Informing sites about performance and contractual issues
• Serving as a site’s contact for communicating with PharmaNet/i3, sponsors, and IRBs

PharmaNet/i3'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. To assist with meeting enrollment goals, PharmaNet/i3 offers the expertise of a dedicated patient recruitment team for skilled at choosing the right strategies and tactics for recruiting and retaining the right subjects.

PharmaNet/i3 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, PharmaNet/i3 applies appropriate technology to meet study requirements and train site personnel in the procedures required to achieve optimal results.

If you’re an investigator interested in participating in clinical research trials with PharmaNet/i3, visit our Investigator’s page.