When you’re ready to move your project into clinical study, you’ll get tools, resources and project management services to keep the momentum going at every research milestone and phase—from study design and patient enrollment all the way to analysis and study close-out.
Such support starts with a carefully selected team of experienced clinical project and trial managers who will work with you to document your needs, track against goals, maintain program movement and measure success.
Following team selection, you’ll enjoy a seamless transition into efficient study strategy and design, and study start-up activities.
As part of our comprehensive clinical trial management package, you’ll get:
- Start-to-Finish Support from Oncology Specialists: Working from a preapproved budget and timeline, our project managers can coordinate and manage all functions of the study for you—including site qualification, project scope, project meetings, patient enrollment and data delivery. And you get it all from specialists who live, work and breathe in the oncology space. After all, as a dedicated CRO that only works in oncology, it’s entirely our niche.
- Timely Response: We know that every project is sacred to you, and that clear communication is integral to the success of each and every clinical trial. That’s why we craft a detailed communication plan and share it with all key project team members—and maintain close communications with our clients, sites and vendors at every juncture of your drug’s journey. We respond rapidly to requests, provide frequent status reports, share your expectations with our greater team, and ensure your satisfaction at every step.
- Comprehensive Risk Management: To minimize delays, our risk management specialists enact proactive solutions to potential difficulties—anticipating scenarios and crafting preapproved response protocols for any outcome. When issues arise, we quickly address and resolve them by identifying their cause and putting in place any needed procedures and processes.